| geneid | 23057 |
|---|---|
| ensemblid | ENSG00000157064.11 |
| hgncid | 16789 |
| symbol | NMNAT2 |
| name | nicotinamide nucleotide adenylyltransferase 2 |
| refseq_nuc | NM_015039.4 |
| refseq_prot | NP_055854.1 |
| ensembl_nuc | ENST00000287713.7 |
| ensembl_prot | ENSP00000287713.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 183248237 |
| end | 183418380 |
| strand | - |
| ver | v1.2 |
| region | chr1:183248237-183418380 |
| region5000 | chr1:183243237-183423380 |
| regionname0 | NMNAT2_chr1_183248237_183418380 |
| regionname5000 | NMNAT2_chr1_183243237_183423380 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 307 | 258 | 84 | 54 | 72 | 16 | 30 | 56 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 924 | 255 | 82 | 54 | 71 | 16 | 30 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| c0002 | 0/0 | 924 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| c0003 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4505 | 20 | 1 | 6 | 10 | 1 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0002 | 1/0 | 4518 | 19 | 6 | 5 | 3 | 3 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0003 | 0/0 | 4516 | 18 | 1 | 8 | 5 | 2 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0004 | 0/0 | 4520 | 13 | 5 | 3 | 3 | 2 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0005 | 0/0 | 4514 | 10 | 4 | 2 | 1 | 1 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0006 | 0/0 | 4505 | 9 | 1 | 0 | 7 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0007 | 0/0 | 4503 | 7 | 0 | 0 | 7 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0008 | 0/0 | 4507 | 7 | 0 | 2 | 0 | 4 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0009 | 0/0 | 4520 | 7 | 4 | 0 | 2 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0010 | 0/0 | 4503 | 6 | 0 | 5 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0011 | 0/0 | 4505 | 6 | 6 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0012 | 0/0 | 4522 | 6 | 1 | 2 | 1 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0013 | 0/0 | 4505 | 5 | 0 | 2 | 3 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0014 | 0/0 | 4510 | 5 | 0 | 0 | 5 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0015 | 0/0 | 4516 | 5 | 0 | 2 | 3 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0016 | 0/0 | 4512 | 5 | 5 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0017 | 0/0 | 4505 | 4 | 4 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0018 | 0/0 | 4518 | 4 | 0 | 1 | 1 | 1 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0019 | 0/0 | 4503 | 3 | 0 | 0 | 3 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0020 | 0/0 | 4512 | 3 | 1 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0021 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0022 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0023 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0024 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0025 | 0/0 | 4497 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0026 | 0/0 | 4509 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0027 | 0/0 | 4507 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0028 | 0/0 | 4505 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0029 | 0/0 | 4505 | 2 | 0 | 0 | 1 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0030 | 0/0 | 4503 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0031 | 0/0 | 4501 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0032 | 0/0 | 4507 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0033 | 0/0 | 4505 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0034 | 0/0 | 4509 | 2 | 0 | 0 | 0 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0035 | 0/0 | 4501 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0036 | 0/0 | 4522 | 2 | 0 | 0 | 0 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0037 | 0/0 | 4518 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0038 | 0/0 | 4516 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0039 | 0/0 | 4514 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0040 | 0/0 | 4516 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0041 | 0/0 | 4514 | 2 | 1 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0042 | 0/0 | 4520 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0043 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0044 | 0/0 | 4519 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0045 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0046 | 0/0 | 4501 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0047 | 0/0 | 4511 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0048 | 0/0 | 4507 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0049 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0050 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0051 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0052 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0053 | 0/0 | 4507 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0054 | 0/0 | 4518 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0055 | 0/0 | 4543 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0056 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0057 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0058 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0059 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0060 | 0/0 | 4505 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0061 | 0/0 | 4513 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0062 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0063 | 0/0 | 4507 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0064 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0065 | 0/0 | 4505 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0066 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0067 | 0/0 | 4505 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0068 | 0/0 | 4511 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0069 | 0/0 | 4507 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0070 | 0/0 | 4503 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0071 | 0/0 | 4510 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0072 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0073 | 0/0 | 4502 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0074 | 0/0 | 4508 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0075 | 0/0 | 4514 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0076 | 0/0 | 4518 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0077 | 0/0 | 4522 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0078 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0079 | 0/1 | 4518 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0080 | 0/0 | 4520 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0081 | 0/0 | 4512 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0082 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0083 | 0/0 | 4508 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0084 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0085 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0086 | 0/0 | 4515 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0087 | 0/0 | 4513 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0088 | 0/0 | 4512 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0089 | 0/0 | 4518 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0090 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0091 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0092 | 0/0 | 4514 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0093 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| t0094 | 0/0 | 4510 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 924 | 255 | 82 | 54 | 71 | 16 | 30 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0002 | 0/0 | 924 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0003 | 0/0 | 924 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5428 | 20 | 1 | 6 | 10 | 1 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0002 | 1/0 | 5441 | 19 | 6 | 5 | 3 | 3 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0003 | 0/0 | 5439 | 17 | 0 | 8 | 5 | 2 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0004 | 0/0 | 5443 | 13 | 5 | 3 | 3 | 2 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0005 | 0/0 | 5437 | 10 | 4 | 2 | 1 | 1 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0006 | 0/0 | 5428 | 9 | 1 | 0 | 7 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0007 | 0/0 | 5426 | 7 | 0 | 0 | 7 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0008 | 0/0 | 5430 | 7 | 0 | 2 | 0 | 4 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0009 | 0/0 | 5443 | 7 | 4 | 0 | 2 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0010 | 0/0 | 5426 | 6 | 0 | 5 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0011 | 0/0 | 5428 | 6 | 6 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0012 | 0/0 | 5445 | 6 | 1 | 2 | 1 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0013 | 0/0 | 5428 | 5 | 0 | 2 | 3 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0014 | 0/0 | 5433 | 5 | 0 | 0 | 5 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0015 | 0/0 | 5439 | 4 | 0 | 2 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0016 | 0/0 | 5435 | 5 | 5 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0017 | 0/0 | 5428 | 4 | 4 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0018 | 0/0 | 5441 | 4 | 0 | 1 | 1 | 1 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0019 | 0/0 | 5426 | 3 | 0 | 0 | 3 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0020 | 0/0 | 5435 | 3 | 1 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0021 | 0/0 | 5430 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0022 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0023 | 0/0 | 5426 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0024 | 0/0 | 5430 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0025 | 0/0 | 5420 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0026 | 0/0 | 5432 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0027 | 0/0 | 5430 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0028 | 0/0 | 5428 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0029 | 0/0 | 5428 | 2 | 0 | 0 | 1 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0030 | 0/0 | 5426 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0031 | 0/0 | 5424 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0032 | 0/0 | 5430 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0033 | 0/0 | 5428 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0034 | 0/0 | 5432 | 2 | 0 | 0 | 0 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0035 | 0/0 | 5424 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0036 | 0/0 | 5445 | 2 | 0 | 0 | 0 | 0 | 2 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0037 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0038 | 0/0 | 5439 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0039 | 0/0 | 5437 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0040 | 0/0 | 5439 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0041 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0042 | 0/0 | 5443 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0043 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0044 | 0/0 | 5442 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0045 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0046 | 0/0 | 5424 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0047 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0048 | 0/0 | 5430 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0049 | 0/0 | 5416 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0050 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0051 | 0/0 | 5426 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0052 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0053 | 0/0 | 5430 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0054 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0055 | 0/0 | 5466 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0056 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0057 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0058 | 0/0 | 5432 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0059 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0060 | 0/0 | 5428 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0061 | 0/0 | 5436 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0062 | 0/0 | 5432 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0063 | 0/0 | 5430 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0064 | 0/0 | 5426 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0065 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0066 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0067 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0068 | 0/0 | 5434 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0069 | 0/0 | 5430 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0070 | 0/0 | 5426 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0071 | 0/0 | 5433 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0072 | 0/0 | 5426 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0073 | 0/0 | 5425 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0074 | 0/0 | 5431 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0075 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0076 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0077 | 0/0 | 5445 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0078 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0079 | 0/1 | 5441 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0080 | 0/0 | 5443 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0081 | 0/0 | 5435 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0082 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0083 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0084 | 0/0 | 5429 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0085 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0086 | 0/0 | 5438 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0087 | 0/0 | 5436 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0088 | 0/0 | 5435 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0089 | 0/0 | 5441 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0090 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0091 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0092 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0093 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0001t0094 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0002t0003 | 0/0 | 5439 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0002t0041 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| a0001c0003t0015 | 0/0 | 5439 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | copy fasta | chr1 | 183243237 | 183423380 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0012g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0013g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0013g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0013g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0014g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0015g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0016g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0016g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0016g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0016g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0017g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0018g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0018g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0019g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0019g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0020g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0020g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0020g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0021g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0022g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0022g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0023g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0023g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0024g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0024g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0025g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0025g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0026g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0026g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0027g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0027g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0028g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0028g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0029g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0029g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0030g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0030g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0031g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0031g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0032g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0032g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0033g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0033g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0034g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0034g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0035g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0035g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0036g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0036g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0037g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0037g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0038g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0038g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0039g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0039g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0040g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0040g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0041g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0042g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0042g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0043g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0044g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0045g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0046g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0047g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0048g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0049g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0050g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0051g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0052g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0053g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0054g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0055g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0056g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0057g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0058g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0059g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0060g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0061g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0062g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0063g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0064g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0065g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0066g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0067g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0068g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0069g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0070g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0071g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0072g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0073g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0074g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0075g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0076g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0077g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0078g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0079g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0080g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0081g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0082g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0083g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0084g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0085g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0086g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0087g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0088g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0089g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0090g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0091g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0092g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0093g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0001t0094g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0002t0041g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| a0001c0003t0015g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | GBR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0156 | EUR | GBR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00140 | hp1 | a0001 | c0001 | t0008 | g0135 | EUR | GBR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0054 | EUR | GBR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00280 | hp2 | a0001 | c0001 | t0018 | g0167 | EUR | FIN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00423 | hp1 | a0001 | c0001 | t0018 | g0111 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0007 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00438 | hp1 | a0001 | c0001 | t0019 | g0191 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00609 | hp1 | a0001 | c0001 | t0075 | g0063 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00609 | hp2 | a0001 | c0001 | t0080 | g0053 | EAS | CHS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00735 | hp2 | a0001 | c0001 | t0013 | g0067 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0126 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01069 | hp1 | a0001 | c0001 | t0050 | g0018 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01071 | hp1 | a0001 | c0001 | t0018 | g0159 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01081 | hp1 | a0001 | c0001 | t0015 | g0204 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01081 | hp2 | a0001 | c0001 | t0012 | g0109 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01099 | hp1 | a0001 | c0001 | t0057 | g0249 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0241 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0157 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0028 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01109 | hp1 | a0001 | c0001 | t0065 | g0134 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01109 | hp2 | a0001 | c0001 | t0030 | g0169 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01167 | hp1 | a0001 | c0001 | t0035 | g0161 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01169 | hp1 | a0001 | c0001 | t0035 | g0031 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01192 | hp2 | a0001 | c0001 | t0032 | g0184 | AMR | PUR | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01257 | hp2 | a0001 | c0001 | t0010 | g0026 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0057 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0207 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01346 | hp2 | a0001 | c0001 | t0084 | g0223 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0209 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01361 | hp1 | a0001 | c0001 | t0077 | g0193 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0119 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0133 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0121 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0122 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | IBS | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01884 | hp1 | a0001 | c0001 | t0056 | g0151 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0059 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01891 | hp2 | a0001 | c0001 | t0033 | g0246 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01952 | hp2 | a0001 | c0001 | t0072 | g0010 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01978 | hp1 | a0001 | c0001 | t0039 | g0214 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01978 | hp2 | a0001 | c0001 | t0039 | g0050 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01981 | hp1 | a0001 | c0001 | t0010 | g0009 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01981 | hp2 | a0001 | c0001 | t0063 | g0141 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01993 | hp1 | a0001 | c0001 | t0064 | g0027 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0092 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0192 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02055 | hp2 | a0001 | c0001 | t0074 | g0102 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02074 | hp1 | a0001 | c0001 | t0088 | g0170 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02074 | hp2 | a0001 | c0001 | t0078 | g0043 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02145 | hp1 | a0001 | c0001 | t0027 | g0185 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02148 | hp1 | a0001 | c0001 | t0012 | g0215 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0098 | EAS | CDX | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02155 | hp2 | a0001 | c0001 | t0029 | g0181 | EAS | CDX | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02258 | hp1 | a0001 | c0001 | t0044 | g0196 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02258 | hp2 | a0001 | c0001 | t0025 | g0016 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02280 | hp1 | a0001 | c0001 | t0085 | g0198 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0002 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02451 | hp1 | a0001 | c0001 | t0093 | g0115 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02451 | hp2 | a0001 | c0001 | t0092 | g0003 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02523 | hp1 | a0001 | c0001 | t0007 | g0069 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02572 | hp1 | a0001 | c0001 | t0024 | g0087 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02602 | hp1 | a0001 | c0001 | t0068 | g0208 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02622 | hp1 | a0001 | c0001 | t0028 | g0218 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02622 | hp2 | a0001 | c0001 | t0032 | g0108 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0255 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0147 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02698 | hp1 | a0001 | c0001 | t0036 | g0189 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02717 | hp2 | a0001 | c0001 | t0024 | g0099 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02723 | hp1 | a0001 | c0001 | t0082 | g0034 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02723 | hp2 | a0001 | c0001 | t0067 | g0123 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0171 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02809 | hp2 | a0001 | c0001 | t0094 | g0248 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02818 | hp2 | a0001 | c0001 | t0042 | g0179 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0144 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02886 | hp2 | a0001 | c0001 | t0027 | g0235 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0254 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0105 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02896 | hp2 | a0001 | c0001 | t0037 | g0252 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0107 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02965 | hp1 | a0001 | c0001 | t0042 | g0058 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02965 | hp2 | a0001 | c0001 | t0058 | g0237 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0176 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03017 | hp1 | a0001 | c0001 | t0034 | g0088 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03017 | hp2 | a0001 | c0001 | t0071 | g0025 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03041 | hp1 | a0001 | c0001 | t0016 | g0175 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03041 | hp2 | a0001 | c0001 | t0045 | g0146 | AFR | GWD | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0247 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03139 | hp2 | a0001 | c0001 | t0021 | g0083 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03209 | hp1 | a0001 | c0001 | t0066 | g0116 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0194 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03225 | hp1 | a0001 | c0001 | t0023 | g0148 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03225 | hp2 | a0001 | c0001 | t0033 | g0110 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03239 | hp1 | a0001 | c0001 | t0087 | g0038 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03239 | hp2 | a0001 | c0001 | t0081 | g0200 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0256 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03490 | hp1 | a0001 | c0001 | t0010 | g0066 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03490 | hp2 | a0001 | c0001 | t0012 | g0155 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03516 | hp1 | a0001 | c0001 | t0022 | g0024 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0103 | AFR | ESN | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03688 | hp1 | a0001 | c0001 | t0041 | g0089 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03688 | hp2 | a0001 | c0001 | t0052 | g0051 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03704 | hp2 | a0001 | c0001 | t0055 | g0188 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03710 | hp1 | a0001 | c0001 | t0062 | g0225 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03710 | hp2 | a0001 | c0001 | t0061 | g0118 | SAS | PJL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03831 | hp2 | a0001 | c0001 | t0053 | g0180 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0042 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0039 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04115 | hp1 | a0001 | c0001 | t0029 | g0182 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04115 | hp2 | a0001 | c0001 | t0054 | g0060 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04184 | hp1 | a0001 | c0001 | t0036 | g0231 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04184 | hp2 | a0001 | c0001 | t0034 | g0091 | SAS | BEB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04199 | hp1 | a0001 | c0001 | t0086 | g0206 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04204 | hp1 | a0001 | c0001 | t0070 | g0113 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG04204 | hp2 | a0001 | c0001 | t0018 | g0197 | SAS | STU | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18522 | hp1 | a0001 | c0001 | t0048 | g0174 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18906 | hp1 | a0001 | c0001 | t0091 | g0257 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0240 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18943 | hp1 | a0001 | c0001 | t0015 | g0040 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18945 | hp1 | a0001 | c0001 | t0083 | g0093 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0195 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18946 | hp1 | a0001 | c0001 | t0060 | g0048 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18946 | hp2 | a0001 | c0001 | t0020 | g0096 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18947 | hp1 | a0001 | c0001 | t0006 | g0097 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18948 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18950 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18950 | hp2 | a0001 | c0001 | t0031 | g0056 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18953 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0023 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18956 | hp2 | a0001 | c0001 | t0015 | g0238 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18964 | hp1 | a0001 | c0001 | t0031 | g0131 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18964 | hp2 | a0001 | c0001 | t0020 | g0095 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18968 | hp2 | a0001 | c0001 | t0014 | g0072 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18970 | hp2 | a0001 | c0001 | t0051 | g0081 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18975 | hp1 | a0001 | c0001 | t0038 | g0079 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18977 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18980 | hp1 | a0001 | c0001 | t0059 | g0162 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18983 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA18983 | hp2 | a0001 | c0001 | t0014 | g0071 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19000 | hp2 | a0001 | c0001 | t0013 | g0129 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19004 | hp1 | a0001 | c0001 | t0014 | g0070 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19005 | hp1 | a0001 | c0001 | t0009 | g0078 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19007 | hp1 | a0001 | c0001 | t0019 | g0052 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19007 | hp2 | a0001 | c0003 | t0015 | g0224 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19010 | hp1 | a0001 | c0001 | t0040 | g0094 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19012 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19030 | hp1 | a0001 | c0001 | t0026 | g0004 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19030 | hp2 | a0001 | c0001 | t0076 | g0234 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19043 | hp1 | a0001 | c0001 | t0049 | g0172 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19043 | hp2 | a0001 | c0001 | t0026 | g0117 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19063 | hp2 | a0001 | c0001 | t0038 | g0190 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19064 | hp1 | a0001 | c0001 | t0069 | g0008 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19064 | hp2 | a0001 | c0001 | t0012 | g0080 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19086 | hp1 | a0001 | c0001 | t0073 | g0033 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19088 | hp1 | a0001 | c0001 | t0019 | g0012 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19088 | hp2 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0173 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA19240 | hp2 | a0001 | c0001 | t0047 | g0075 | AFR | YRI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0145 | AFR | ASW | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | ASW | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0061 | EUR | TSI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20752 | hp2 | a0001 | c0001 | t0009 | g0232 | EUR | TSI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0154 | EUR | TSI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0055 | EUR | TSI | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01123 | hp1 | a0001 | c0001 | t0040 | g0205 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG01123 | hp2 | a0001 | c0001 | t0089 | g0085 | AMR | CLM | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02109 | hp1 | a0001 | c0001 | t0016 | g0253 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02486 | hp1 | a0001 | c0001 | t0025 | g0014 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02486 | hp2 | a0001 | c0001 | t0037 | g0068 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02559 | hp1 | a0001 | c0001 | t0090 | g0226 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG02559 | hp2 | a0001 | c0001 | t0046 | g0150 | AFR | ACB | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03471 | hp1 | a0001 | c0001 | t0043 | g0074 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | USA | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | USA | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA21309 | hp1 | a0001 | c0002 | t0041 | g0230 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| NA21309 | hp2 | a0001 | c0001 | t0030 | g0017 | AFR | LWK | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0079 | g0177 | REF | REF | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0186 | REF | REF | NMNAT2_chr1_183243237_183423380 | NMNAT2 | chr1 | 183243237 | 183423380 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183252743
|
C | T | 1 | a0001c0002 | 2 | HG02970.hp2 NA21309.hp1 |
splice_region_variant&synonymous_variant | LOW | c.822G>A | p.Arg274Arg | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 935/5441 | 822/924 | 274/307 | chr1 | 183252743 | ||
| chr1:183284732
|
C | A | 1 | a0001c0003 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.507G>T | p.Pro169Pro | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 6/11 | 620/5441 | 507/924 | 169/307 | chr1 | 183284732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183248244
|
G | A | 3 | a0001c0001t0007a0001c0001t0059a0001c0001t0060 | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4397C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 4397 | chr1 | 183248244 | |||||
| chr1:183248537
|
G | A | 1 | a0001c0001t0082 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4104C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 4104 | chr1 | 183248537 | |||||
| chr1:183248633
|
T | A | 1 | a0001c0001t0055 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4008A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 4008 | chr1 | 183248633 | |||||
| chr1:183248891
|
A | AGT | 13 | a0001c0001t0009a0001c0001t0012a0001c0001t0027others(10): Show | 27 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3748_*3749dupAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3749 | chr1 | 183248891 | |||||
| chr1:183248891
|
A | AGTGT | 7 | a0001c0001t0014a0001c0001t0026a0001c0001t0040others(4): Show | 13 | HG01123.hp1 HG01361.hp1 HG02074.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3746_*3749dupACAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3749 | chr1 | 183248891 | |||||
| chr1:183248891
|
A | AGTGTGT | 3 | a0001c0001t0052a0001c0001t0075a0001c0001t0080 | 3 | HG00609.hp1 HG00609.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3744_*3749dupACAC others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3749 | chr1 | 183248891 | |||||
| chr1:183248891
|
AGT | A | 28 | a0001c0001t0001a0001c0001t0006a0001c0001t0011others(25): Show | 74 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3748_*3749delAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3748 | chr1 | 183248891 | |||||
| chr1:183248891
|
AGTGT | A | 11 | a0001c0001t0007a0001c0001t0015a0001c0001t0017others(8): Show | 25 | HG01081.hp1 HG01099.hp2 HG01346.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3746_*3749delACAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3746 | chr1 | 183248891 | |||||
| chr1:183248891
|
AGTGTGT | A | 4 | a0001c0001t0021a0001c0001t0023a0001c0001t0031others(1): Show | 7 | HG02647.hp2 HG03041.hp2 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3744_*3749delACAC others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3744 | chr1 | 183248891 | |||||
| chr1:183248891
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0025a0001c0001t0046 | 3 | HG02258.hp2 HG02486.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3740_*3749delACAC others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3740 | chr1 | 183248891 | |||||
| chr1:183248891
|
AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0049 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3734_*3749delACAC others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3734 | chr1 | 183248891 | |||||
| chr1:183248893
|
T | A | 3 | a0001c0001t0008a0001c0001t0058a0001c0001t0065 | 9 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3748A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3748 | chr1 | 183248893 | |||||
| chr1:183248895
|
T | A | 8 | a0001c0001t0001a0001c0001t0019a0001c0001t0033others(5): Show | 30 | HG00280.hp1 HG00438.hp1 HG01261.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3746A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3746 | chr1 | 183248895 | |||||
| chr1:183248897
|
T | A | 1 | a0001c0001t0064 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3744A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3744 | chr1 | 183248897 | |||||
| chr1:183248899
|
T | A | 1 | a0001c0001t0031 | 2 | NA18950.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3742A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3742 | chr1 | 183248899 | |||||
| chr1:183249024
|
T | C | 1 | a0001c0001t0082 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3617A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3617 | chr1 | 183249024 | |||||
| chr1:183249127
|
G | A | 3 | a0001c0001t0007a0001c0001t0059a0001c0001t0060 | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3514C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3514 | chr1 | 183249127 | |||||
| chr1:183249242
|
C | T | 1 | a0001c0001t0070 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3399G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3399 | chr1 | 183249242 | |||||
| chr1:183249324
|
A | T | 1 | a0001c0001t0076 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3317T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3317 | chr1 | 183249324 | |||||
| chr1:183249343
|
C | G | 3 | a0001c0001t0007a0001c0001t0059a0001c0001t0060 | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3298G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 3298 | chr1 | 183249343 | |||||
| chr1:183249682
|
C | CGT | 6 | a0001c0001t0004a0001c0001t0012a0001c0001t0015others(3): Show | 29 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2957_*2958dupAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2958 | chr1 | 183249682 | |||||
| chr1:183249682
|
C | CGTGT | 3 | a0001c0001t0036a0001c0001t0037a0001c0001t0042 | 6 | HG02486.hp2 HG02698.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2955_*2958dupACAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2958 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGT | C | 6 | a0001c0001t0003a0001c0001t0021a0001c0001t0078others(3): Show | 23 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2957_*2958delAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2957 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGTGT | C | 11 | a0001c0001t0005a0001c0001t0016a0001c0001t0045others(8): Show | 24 | HG00609.hp2 HG01261.hp2 HG01358.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2955_*2958delACAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2955 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGTGTGT | C | 17 | a0001c0001t0017a0001c0001t0020a0001c0001t0022others(14): Show | 26 | HG01123.hp1 HG01192.hp2 HG02074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2953_*2958delACAC others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2953 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGTGTGTG others(1): Show |
C | 20 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(17): Show | 73 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2951_*2958delACAC others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2951 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGTGTGTG others(3): Show |
C | 12 | a0001c0001t0019a0001c0001t0026a0001c0001t0027others(9): Show | 18 | HG00438.hp1 HG00609.hp1 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2949_*2958delACAC others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2949 | chr1 | 183249682 | |||||
| chr1:183249682
|
CGTGTGTG others(5): Show |
C | 7 | a0001c0001t0010a0001c0001t0014a0001c0001t0029others(4): Show | 18 | HG01106.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2947_*2958delACAC others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2947 | chr1 | 183249682 | |||||
| chr1:183249721
|
GTGTGTGT others(4): Show |
G | 1 | a0001c0001t0073 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2909_*2919delACAC others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2909 | chr1 | 183249721 | |||||
| chr1:183249729
|
GTGT | G | 4 | a0001c0001t0066a0001c0001t0071a0001c0001t0086others(1): Show | 4 | HG03017.hp2 HG03209.hp1 HG03239.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2909_*2911delACA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2909 | chr1 | 183249729 | |||||
| chr1:183249888
|
A | G | 8 | a0001c0001t0016a0001c0001t0042a0001c0001t0056others(5): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2753T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2753 | chr1 | 183249888 | |||||
| chr1:183250166
|
G | A | 1 | a0001c0001t0088 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2475C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2475 | chr1 | 183250166 | |||||
| chr1:183250213
|
A | T | 12 | a0001c0001t0001a0001c0001t0008a0001c0001t0019others(9): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2428T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2428 | chr1 | 183250213 | |||||
| chr1:183250219
|
C | T | 3 | a0001c0001t0007a0001c0001t0059a0001c0001t0060 | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2422G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 2422 | chr1 | 183250219 | |||||
| chr1:183250738
|
C | T | 2 | a0001c0001t0030a0001c0001t0057 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1903G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1903 | chr1 | 183250738 | |||||
| chr1:183250836
|
C | T | 1 | a0001c0001t0076 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1805G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1805 | chr1 | 183250836 | |||||
| chr1:183250839
|
G | A | 1 | a0001c0001t0058 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1802C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1802 | chr1 | 183250839 | |||||
| chr1:183251322
|
AC | A | 8 | a0001c0001t0016a0001c0001t0042a0001c0001t0056others(5): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1318delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1318 | chr1 | 183251322 | |||||
| chr1:183251343
|
A | G | 3 | a0001c0001t0007a0001c0001t0059a0001c0001t0060 | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1298T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1298 | chr1 | 183251343 | |||||
| chr1:183251404
|
T | C | 8 | a0001c0001t0006a0001c0001t0013a0001c0001t0034others(5): Show | 22 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1237A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1237 | chr1 | 183251404 | |||||
| chr1:183251443
|
G | C | 2 | a0001c0001t0072a0001c0001t0073 | 2 | HG01952.hp2 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1198 | chr1 | 183251443 | |||||
| chr1:183251503
|
T | C | 1 | a0001c0001t0089 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1138 | chr1 | 183251503 | |||||
| chr1:183251608
|
G | C | 1 | a0001c0001t0013 | 5 | HG00735.hp2 HG01106.hp1 HG02015.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1033 | chr1 | 183251608 | |||||
| chr1:183251640
|
C | T | 1 | a0001c0001t0058 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1001G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 1001 | chr1 | 183251640 | |||||
| chr1:183251802
|
A | G | 63 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(60): Show | 145 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*839T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 839 | chr1 | 183251802 | |||||
| chr1:183251840
|
A | G | 2 | a0001c0001t0030a0001c0001t0057 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*801T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 801 | chr1 | 183251840 | |||||
| chr1:183251855
|
TTGC | T | 60 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(57): Show | 138 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*783_*785delGCA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 783 | chr1 | 183251855 | |||||
| chr1:183251878
|
G | A | 8 | a0001c0001t0016a0001c0001t0042a0001c0001t0056others(5): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*763C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 763 | chr1 | 183251878 | |||||
| chr1:183251932
|
C | CGT | 8 | a0001c0001t0016a0001c0001t0042a0001c0001t0056others(5): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*707_*708dupAC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 708 | chr1 | 183251932 | |||||
| chr1:183252211
|
A | G | 8 | a0001c0001t0016a0001c0001t0042a0001c0001t0056others(5): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*430T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 430 | chr1 | 183252211 | |||||
| chr1:183252249
|
G | GGGGCACC others(32): Show |
1 | a0001c0001t0055 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*391_*392insATCCTC others(33): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 391 | chr1 | 183252249 | |||||
| chr1:183252257
|
A | T | 1 | a0001c0001t0043 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 384 | chr1 | 183252257 | |||||
| chr1:183252270
|
T | C | 7 | a0001c0001t0016a0001c0001t0042a0001c0001t0090others(4): Show | 12 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*371A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 371 | chr1 | 183252270 | |||||
| chr1:183252351
|
A | G | 1 | a0001c0001t0054 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*290T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 290 | chr1 | 183252351 | |||||
| chr1:183252498
|
C | T | 22 | a0001c0001t0010a0001c0001t0017a0001c0001t0021others(19): Show | 39 | HG01069.hp1 HG01106.hp2 HG01257.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 11/11 | 143 | chr1 | 183252498 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:183252764
|
A | G | 1 | a0001c0001t0007g0021 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.822-21T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183252764 | ||||||
| chr1:183252878
|
G | A | 136 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.822-135C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183252878 | ||||||
| chr1:183253004
|
A | G | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.822-261T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253004 | ||||||
| chr1:183253147
|
G | T | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.822-404C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253147 | ||||||
| chr1:183253543
|
A | G | 22 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.822-800T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253543 | ||||||
| chr1:183253847
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.822-1104C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253847 | ||||||
| chr1:183253904
|
C | CGT | 9 | a0001c0001t0005g0077a0001c0001t0009g0120a0001c0001t0017g0171others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.822-1163_822-1162d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
C | CGTGT | 7 | a0001c0001t0009g0143a0001c0001t0017g0002a0001c0001t0017g0173others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.822-1165_822-1162d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGT | C | 43 | a0001c0001t0001g0045a0001c0001t0002g0041a0001c0001t0002g0086others(40): Show | 43 | HG00280.hp2 HG00609.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.822-1163_822-1162d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGT | C | 33 | a0001c0001t0001g0142a0001c0001t0002g0013a0001c0001t0003g0032others(30): Show | 33 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.822-1165_822-1162d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGTGT | C | 7 | a0001c0001t0001g0036a0001c0001t0033g0246a0001c0001t0034g0088others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.822-1167_822-1162d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGTGTG others(1): Show |
C | 60 | a0001c0001t0001g0035a0001c0001t0001g0101a0001c0001t0001g0124others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.822-1169_822-1162d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.822-1171_822-1162d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGTGTG others(5): Show |
C | 3 | a0001c0001t0006g0098a0001c0001t0019g0052a0001c0001t0093g0115 | 3 | HG02155.hp1 HG02451.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.822-1173_822-1162d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253904
|
CGTGTGTG others(7): Show |
C | 17 | a0001c0001t0011g0103a0001c0001t0011g0105a0001c0001t0011g0106others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.822-1175_822-1162d others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253904 | ||||||
| chr1:183253945
|
A | G | 2 | a0001c0001t0002g0001a0001c0001t0044g0196 | 3 | HG01069.hp2 HG01071.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.822-1202T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253945 | ||||||
| chr1:183253947
|
G | A | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.822-1204C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183253947 | ||||||
| chr1:183254052
|
A | C | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-1309T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254052 | ||||||
| chr1:183254136
|
G | A | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-1393C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254136 | ||||||
| chr1:183254273
|
G | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.822-1530C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254273 | ||||||
| chr1:183254375
|
T | G | 1 | a0001c0001t0002g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.822-1632A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254375 | ||||||
| chr1:183254418
|
TTTTG | T | 53 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(50): Show | 53 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.822-1679_822-1676d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254418 | ||||||
| chr1:183254418
|
TTTTGTTT others(1): Show |
T | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-1683_822-1676d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254418 | ||||||
| chr1:183254585
|
A | G | 1 | a0001c0001t0070g0113 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.822-1842T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254585 | ||||||
| chr1:183254678
|
C | A | 2 | a0001c0001t0007g0019a0001c0001t0007g0020 | 2 | NA18950.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.822-1935G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254678 | ||||||
| chr1:183254724
|
A | G | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-1981T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254724 | ||||||
| chr1:183254789
|
G | C | 2 | a0001c0001t0005g0076a0001c0001t0079g0177 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.822-2046C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254789 | ||||||
| chr1:183254891
|
C | T | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.822-2148G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183254891 | ||||||
| chr1:183255050
|
A | T | 1 | a0001c0001t0015g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.822-2307T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255050 | ||||||
| chr1:183255065
|
T | C | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2322A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255065 | ||||||
| chr1:183255255
|
A | T | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.822-2512T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255255 | ||||||
| chr1:183255258
|
C | T | 1 | a0001c0002t0041g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.822-2515G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255258 | ||||||
| chr1:183255650
|
TTATTCCT others(5): Show |
T | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2919_822-2908d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255650 | ||||||
| chr1:183255662
|
G | GT | 19 | a0001c0001t0001g0228a0001c0001t0001g0245a0001c0001t0007g0019others(16): Show | 19 | HG01099.hp1 HG01257.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.822-2920dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255662 | ||||||
| chr1:183255662
|
G | T | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.822-2919C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255662 | ||||||
| chr1:183255662
|
GT | G | 123 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(120): Show | 124 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.822-2920delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255662 | ||||||
| chr1:183255662
|
GTT | G | 8 | a0001c0001t0002g0153a0001c0001t0003g0156a0001c0001t0003g0187others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.822-2921_822-2920d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255662 | ||||||
| chr1:183255663
|
T | G | 21 | a0001c0001t0001g0227a0001c0001t0016g0175a0001c0001t0016g0194others(18): Show | 21 | HG00280.hp1 HG00438.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.822-2920A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255663 | ||||||
| chr1:183255666
|
T | A | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2923A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255666 | ||||||
| chr1:183255667
|
T | A | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2924A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255667 | ||||||
| chr1:183255668
|
T | A | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2925A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255668 | ||||||
| chr1:183255798
|
G | A | 1 | a0001c0001t0029g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.822-3055C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255798 | ||||||
| chr1:183255799
|
G | A | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-3056C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255799 | ||||||
| chr1:183255811
|
A | C | 12 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(9): Show | 12 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.822-3068T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255811 | ||||||
| chr1:183255851
|
A | G | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.822-3108T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255851 | ||||||
| chr1:183255954
|
G | A | 114 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.822-3211C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183255954 | ||||||
| chr1:183256176
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.822-3433C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256176 | ||||||
| chr1:183256226
|
C | T | 43 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.822-3483G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256226 | ||||||
| chr1:183256248
|
A | T | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.822-3505T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256248 | ||||||
| chr1:183256276
|
G | A | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.822-3533C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256276 | ||||||
| chr1:183256309
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.822-3566A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256309 | ||||||
| chr1:183256340
|
C | T | 43 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.822-3597G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256340 | ||||||
| chr1:183256374
|
A | T | 27 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(24): Show | 27 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.822-3631T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256374 | ||||||
| chr1:183256430
|
A | T | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-3687T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256430 | ||||||
| chr1:183256624
|
A | G | 1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.822-3881T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256624 | ||||||
| chr1:183256799
|
G | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.822-4056C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256799 | ||||||
| chr1:183256810
|
C | T | 1 | a0001c0001t0018g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.822-4067G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256810 | ||||||
| chr1:183256827
|
C | G | 2 | a0001c0001t0002g0158a0001c0001t0018g0159 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.822-4084G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256827 | ||||||
| chr1:183256994
|
G | C | 145 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(142): Show | 145 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.821+4008C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183256994 | ||||||
| chr1:183257087
|
C | T | 1 | a0001c0001t0003g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.821+3915G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257087 | ||||||
| chr1:183257209
|
G | A | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.821+3793C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257209 | ||||||
| chr1:183257300
|
G | C | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.821+3702C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257300 | ||||||
| chr1:183257516
|
T | C | 45 | a0001c0001t0010g0009a0001c0001t0010g0011a0001c0001t0010g0026others(42): Show | 45 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.821+3486A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257516 | ||||||
| chr1:183257591
|
A | G | 28 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(25): Show | 28 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.821+3411T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257591 | ||||||
| chr1:183257786
|
GT | G | 13 | a0001c0001t0016g0175a0001c0001t0016g0194a0001c0001t0016g0253others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.821+3215delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183257786 | ||||||
| chr1:183258063
|
T | C | 1 | a0001c0001t0062g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.821+2939A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258063 | ||||||
| chr1:183258201
|
C | T | 1 | a0001c0001t0015g0241 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.821+2801G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258201 | ||||||
| chr1:183258391
|
A | G | 6 | a0001c0001t0021g0083a0001c0001t0021g0145a0001c0001t0023g0147others(3): Show | 6 | HG02559.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+2611T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258391 | ||||||
| chr1:183258550
|
A | G | 2 | a0001c0001t0072g0010a0001c0001t0073g0033 | 2 | HG01952.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.821+2452T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258550 | ||||||
| chr1:183258557
|
T | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0057 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.821+2445A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258557 | ||||||
| chr1:183258625
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.821+2377C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258625 | ||||||
| chr1:183258626
|
G | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.821+2376C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258626 | ||||||
| chr1:183258634
|
T | C | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+2368A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258634 | ||||||
| chr1:183258656
|
C | A | 1 | a0001c0001t0031g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.821+2346G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258656 | ||||||
| chr1:183258669
|
G | C | 6 | a0001c0001t0002g0082a0001c0001t0004g0178a0001c0001t0004g0233others(3): Show | 6 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+2333C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258669 | ||||||
| chr1:183258966
|
G | A | 1 | a0001c0001t0011g0015 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.821+2036C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183258966 | ||||||
| chr1:183259074
|
C | T | 2 | a0001c0001t0042g0058a0001c0001t0042g0179 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.821+1928G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259074 | ||||||
| chr1:183259171
|
C | T | 43 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.821+1831G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259171 | ||||||
| chr1:183259240
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.821+1762C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259240 | ||||||
| chr1:183259246
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.821+1756T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259246 | ||||||
| chr1:183259341
|
G | A | 3 | a0001c0001t0030g0017a0001c0001t0030g0169a0001c0001t0057g0249 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.821+1661C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259341 | ||||||
| chr1:183259606
|
T | G | 234 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.821+1396A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259606 | ||||||
| chr1:183259606
|
T | TTGTG | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.821+1392_821+1395d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259606 | ||||||
| chr1:183259622
|
T | C | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.821+1380A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259622 | ||||||
| chr1:183259671
|
C | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.821+1331G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259671 | ||||||
| chr1:183259693
|
G | A | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.821+1309C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259693 | ||||||
| chr1:183259745
|
G | A | 2 | a0001c0001t0025g0014a0001c0001t0025g0016 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.821+1257C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259745 | ||||||
| chr1:183259780
|
T | C | 2 | a0001c0001t0005g0104a0001c0001t0005g0112 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.821+1222A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259780 | ||||||
| chr1:183259783
|
T | C | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.821+1219A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259783 | ||||||
| chr1:183259851
|
G | A | 114 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.821+1151C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259851 | ||||||
| chr1:183259877
|
G | C | 1 | a0001c0001t0015g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.821+1125C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259877 | ||||||
| chr1:183259926
|
C | T | 32 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(29): Show | 32 | HG00423.hp2 HG00735.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.821+1076G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183259926 | ||||||
| chr1:183260011
|
G | T | 1 | a0001c0001t0005g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.821+991C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260011 | ||||||
| chr1:183260028
|
G | T | 1 | a0001c0001t0004g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.821+974C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260028 | ||||||
| chr1:183260105
|
G | C | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.821+897C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260105 | ||||||
| chr1:183260244
|
T | G | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.821+758A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260244 | ||||||
| chr1:183260436
|
C | A | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.821+566G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260436 | ||||||
| chr1:183260477
|
CT | C | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.821+524delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260477 | ||||||
| chr1:183260486
|
A | C | 117 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.821+516T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260486 | ||||||
| chr1:183260487
|
T | C | 117 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.821+515A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260487 | ||||||
| chr1:183260487
|
T | G | 126 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.821+515A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260487 | ||||||
| chr1:183260733
|
T | G | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.821+269A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260733 | ||||||
| chr1:183260737
|
T | G | 117 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.821+265A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260737 | ||||||
| chr1:183260751
|
G | A | 9 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(6): Show | 9 | HG01167.hp2 HG01515.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.821+251C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260751 | ||||||
| chr1:183260819
|
C | CA | 32 | a0001c0001t0001g0045a0001c0001t0001g0242a0001c0001t0002g0210others(29): Show | 32 | HG00438.hp2 HG01081.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.821+182dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260819 | ||||||
| chr1:183260819
|
C | CAA | 11 | a0001c0001t0007g0021a0001c0001t0017g0002a0001c0001t0017g0171others(8): Show | 11 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.821+181_821+182dup others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260819 | ||||||
| chr1:183260819
|
CA | C | 51 | a0001c0001t0002g0001a0001c0001t0002g0049a0001c0001t0002g0164others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.821+182delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260819 | ||||||
| chr1:183260990
|
T | C | 1 | a0001c0002t0041g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.821+12A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 10/10 | chr1 | 183260990 | ||||||
| chr1:183261381
|
ATCCGC | A | 110 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.652-83_652-79delGC others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261381 | ||||||
| chr1:183261384
|
C | T | 39 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.652-81G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261384 | ||||||
| chr1:183261385
|
G | A | 1 | a0001c0001t0015g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.652-82C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261385 | ||||||
| chr1:183261386
|
C | A | 1 | a0001c0001t0015g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.652-83G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261386 | ||||||
| chr1:183261523
|
C | G | 1 | a0001c0001t0019g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.652-220G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261523 | ||||||
| chr1:183261573
|
G | A | 2 | a0001c0001t0005g0076a0001c0001t0079g0177 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.652-270C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261573 | ||||||
| chr1:183261603
|
C | T | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0039g0214 | 3 | HG01257.hp1 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.652-300G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261603 | ||||||
| chr1:183261845
|
T | C | 1 | a0001c0001t0092g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.652-542A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261845 | ||||||
| chr1:183261899
|
G | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-596C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261899 | ||||||
| chr1:183261923
|
AT | A | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.652-621delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183261923 | ||||||
| chr1:183262099
|
T | A | 2 | a0001c0001t0020g0247a0001c0001t0066g0116 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.652-796A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262099 | ||||||
| chr1:183262123
|
C | G | 29 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(26): Show | 29 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.652-820G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262123 | ||||||
| chr1:183262134
|
T | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.652-831A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262134 | ||||||
| chr1:183262244
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.652-941G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262244 | ||||||
| chr1:183262253
|
G | T | 2 | a0001c0001t0002g0210a0001c0001t0038g0190 | 2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.652-950C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262253 | ||||||
| chr1:183262307
|
GA | G | 238 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.652-1005delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262307 | ||||||
| chr1:183262374
|
A | G | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.652-1071T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262374 | ||||||
| chr1:183262412
|
A | G | 45 | a0001c0001t0010g0009a0001c0001t0010g0011a0001c0001t0010g0026others(42): Show | 45 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.652-1109T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262412 | ||||||
| chr1:183262583
|
A | G | 3 | a0001c0001t0033g0110a0001c0001t0033g0246a0001c0001t0058g0237 | 3 | HG01891.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.652-1280T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262583 | ||||||
| chr1:183262671
|
A | G | 3 | a0001c0001t0025g0014a0001c0001t0025g0016a0001c0001t0050g0018 | 3 | HG01069.hp1 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.652-1368T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262671 | ||||||
| chr1:183262753
|
T | G | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-1450A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262753 | ||||||
| chr1:183262757
|
G | A | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.652-1454C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262757 | ||||||
| chr1:183262767
|
G | A | 1 | a0001c0001t0012g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.652-1464C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262767 | ||||||
| chr1:183262776
|
T | G | 7 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(4): Show | 7 | HG01167.hp2 HG01515.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.652-1473A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262776 | ||||||
| chr1:183262923
|
G | C | 111 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.652-1620C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183262923 | ||||||
| chr1:183263107
|
C | T | 3 | a0001c0001t0033g0110a0001c0001t0033g0246a0001c0001t0058g0237 | 3 | HG01891.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.652-1804G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263107 | ||||||
| chr1:183263420
|
A | G | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.652-2117T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263420 | ||||||
| chr1:183263536
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.652-2233C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263536 | ||||||
| chr1:183263569
|
A | G | 39 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.652-2266T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263569 | ||||||
| chr1:183263650
|
C | CA | 10 | a0001c0001t0002g0149a0001c0001t0007g0019a0001c0001t0007g0020others(7): Show | 10 | HG02109.hp2 HG02523.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-2348dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263650 | ||||||
| chr1:183263815
|
AAAAC | A | 243 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.652-2516_652-2513d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263815 | ||||||
| chr1:183263847
|
T | C | 39 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.652-2544A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263847 | ||||||
| chr1:183263883
|
A | G | 116 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.652-2580T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263883 | ||||||
| chr1:183263929
|
T | C | 3 | a0001c0001t0030g0017a0001c0001t0030g0169a0001c0001t0057g0249 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.652-2626A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183263929 | ||||||
| chr1:183264032
|
G | A | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.652-2729C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264032 | ||||||
| chr1:183264083
|
C | T | 1 | a0001c0001t0007g0022 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.652-2780G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264083 | ||||||
| chr1:183264085
|
T | C | 7 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.652-2782A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264085 | ||||||
| chr1:183264087
|
G | A | 2 | a0001c0001t0081g0200a0001c0001t0086g0206 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.652-2784C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264087 | ||||||
| chr1:183264367
|
C | T | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-3064G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264367 | ||||||
| chr1:183264604
|
C | G | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.652-3301G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264604 | ||||||
| chr1:183264620
|
C | T | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.652-3317G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264620 | ||||||
| chr1:183264669
|
G | A | 1 | a0001c0001t0052g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.652-3366C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264669 | ||||||
| chr1:183264680
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.652-3377C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264680 | ||||||
| chr1:183264697
|
G | T | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-3394C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264697 | ||||||
| chr1:183264701
|
C | T | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.652-3398G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264701 | ||||||
| chr1:183264754
|
C | T | 29 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(26): Show | 29 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.652-3451G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264754 | ||||||
| chr1:183264755
|
G | A | 2 | a0001c0001t0025g0014a0001c0001t0025g0016 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.652-3452C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264755 | ||||||
| chr1:183264911
|
T | C | 1 | a0001c0001t0005g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.652-3608A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264911 | ||||||
| chr1:183264957
|
G | A | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.652-3654C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183264957 | ||||||
| chr1:183265042
|
A | G | 39 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.652-3739T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265042 | ||||||
| chr1:183265080
|
G | T | 2 | a0001c0001t0032g0108a0001c0001t0032g0184 | 2 | HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.652-3777C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265080 | ||||||
| chr1:183265129
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.652-3826G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265129 | ||||||
| chr1:183265172
|
CAAAT | C | 235 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.652-3873_652-3870d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265172 | ||||||
| chr1:183265194
|
C | T | 113 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.652-3891G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265194 | ||||||
| chr1:183265241
|
CTCT | C | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.652-3941_652-3939d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265241 | ||||||
| chr1:183265255
|
CTTCTTTT others(6): Show |
C | 2 | a0001c0001t0062g0225a0001c0001t0071g0025 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.652-3965_652-3953d others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265255 | ||||||
| chr1:183265258
|
CT | C | 111 | a0001c0001t0001g0036a0001c0001t0002g0001a0001c0001t0002g0037others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.652-3956delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265258 | ||||||
| chr1:183265258
|
CTT | C | 52 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0101others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.652-3957_652-3956d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265258 | ||||||
| chr1:183265258
|
CTTTTTTT others(3): Show |
C | 27 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(24): Show | 27 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.652-3965_652-3956d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265258 | ||||||
| chr1:183265261
|
T | C | 1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.652-3958A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265261 | ||||||
| chr1:183265263
|
T | C | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.652-3960A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265263 | ||||||
| chr1:183265291
|
CAG | C | 3 | a0001c0001t0030g0017a0001c0001t0030g0169a0001c0001t0057g0249 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.652-3990_652-3989d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265291 | ||||||
| chr1:183265416
|
G | A | 1 | a0001c0001t0058g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.652-4113C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265416 | ||||||
| chr1:183265560
|
C | T | 2 | a0001c0001t0010g0066a0001c0001t0029g0182 | 2 | HG03490.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.652-4257G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265560 | ||||||
| chr1:183265619
|
C | A | 4 | a0001c0001t0003g0046a0001c0001t0003g0062a0001c0001t0003g0065others(1): Show | 4 | HG00438.hp2 HG02015.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-4316G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265619 | ||||||
| chr1:183265748
|
G | C | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-4445C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265748 | ||||||
| chr1:183265768
|
C | T | 5 | a0001c0001t0022g0240a0001c0001t0024g0087a0001c0001t0028g0218others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.652-4465G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265768 | ||||||
| chr1:183265847
|
C | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-4544G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183265847 | ||||||
| chr1:183266299
|
C | T | 2 | a0001c0001t0018g0167a0001c0001t0037g0068 | 2 | HG00280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.652-4996G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266299 | ||||||
| chr1:183266300
|
A | G | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-4997T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266300 | ||||||
| chr1:183266516
|
G | A | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.652-5213C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266516 | ||||||
| chr1:183266539
|
G | A | 2 | a0001c0001t0032g0108a0001c0001t0032g0184 | 2 | HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.652-5236C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266539 | ||||||
| chr1:183266692
|
T | G | 1 | a0001c0001t0003g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.652-5389A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266692 | ||||||
| chr1:183266804
|
C | T | 1 | a0001c0001t0091g0257 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652-5501G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266804 | ||||||
| chr1:183266829
|
G | A | 2 | a0001c0001t0005g0076a0001c0001t0079g0177 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.652-5526C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266829 | ||||||
| chr1:183266986
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.652-5683G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266986 | ||||||
| chr1:183266987
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.652-5684G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183266987 | ||||||
| chr1:183267093
|
T | C | 4 | a0001c0001t0011g0192a0001c0001t0032g0108a0001c0001t0032g0184others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-5790A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267093 | ||||||
| chr1:183267131
|
C | T | 1 | a0001c0001t0009g0078 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.652-5828G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267131 | ||||||
| chr1:183267327
|
G | T | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-6024C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267327 | ||||||
| chr1:183267532
|
T | C | 33 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(30): Show | 33 | HG00423.hp2 HG00735.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.652-6229A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267532 | ||||||
| chr1:183267572
|
G | C | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-6269C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267572 | ||||||
| chr1:183267614
|
G | C | 4 | a0001c0001t0011g0192a0001c0001t0032g0108a0001c0001t0032g0184others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-6311C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267614 | ||||||
| chr1:183267627
|
G | C | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.652-6324C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267627 | ||||||
| chr1:183267717
|
A | C | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-6414T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267717 | ||||||
| chr1:183267806
|
G | A | 1 | a0001c0001t0071g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.652-6503C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267806 | ||||||
| chr1:183267818
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0012g0215 | 3 | HG01069.hp2 HG01071.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.652-6515G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267818 | ||||||
| chr1:183267856
|
G | A | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-6553C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183267856 | ||||||
| chr1:183268275
|
T | C | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.652-6972A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268275 | ||||||
| chr1:183268289
|
G | A | 1 | a0001c0001t0009g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.652-6986C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268289 | ||||||
| chr1:183268290
|
G | A | 4 | a0001c0001t0011g0192a0001c0001t0032g0108a0001c0001t0032g0184others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-6987C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268290 | ||||||
| chr1:183268291
|
G | A | 1 | a0001c0001t0058g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.652-6988C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268291 | ||||||
| chr1:183268489
|
T | A | 1 | a0001c0001t0040g0205 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.652-7186A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268489 | ||||||
| chr1:183268511
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.652-7208A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268511 | ||||||
| chr1:183268658
|
G | A | 1 | a0001c0001t0058g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.652-7355C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268658 | ||||||
| chr1:183268791
|
C | T | 3 | a0001c0001t0011g0192a0001c0001t0032g0108a0001c0001t0032g0184 | 3 | HG01192.hp2 HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.652-7488G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268791 | ||||||
| chr1:183268805
|
G | A | 111 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.652-7502C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268805 | ||||||
| chr1:183268965
|
C | T | 38 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.652-7662G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268965 | ||||||
| chr1:183268992
|
T | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-7689A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183268992 | ||||||
| chr1:183269018
|
T | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-7715A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269018 | ||||||
| chr1:183269037
|
G | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-7734C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269037 | ||||||
| chr1:183269120
|
T | C | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-7817A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269120 | ||||||
| chr1:183269267
|
C | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-7964G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269267 | ||||||
| chr1:183269393
|
G | A | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.652-8090C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269393 | ||||||
| chr1:183269459
|
C | T | 1 | a0001c0001t0004g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.652-8156G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183269459 | ||||||
| chr1:183270042
|
C | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+8511G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270042 | ||||||
| chr1:183270100
|
A | G | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.651+8453T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270100 | ||||||
| chr1:183270454
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0132 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.651+8099C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270454 | ||||||
| chr1:183270531
|
G | GA | 25 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(22): Show | 25 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.651+8021dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270531 | ||||||
| chr1:183270543
|
A | G | 119 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.651+8010T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270543 | ||||||
| chr1:183270723
|
C | T | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.651+7830G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270723 | ||||||
| chr1:183270768
|
G | A | 1 | a0001c0001t0046g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.651+7785C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183270768 | ||||||
| chr1:183271001
|
C | T | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.651+7552G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271001 | ||||||
| chr1:183271154
|
T | C | 1 | a0001c0001t0003g0187 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.651+7399A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271154 | ||||||
| chr1:183271335
|
C | T | 111 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.651+7218G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271335 | ||||||
| chr1:183271536
|
C | T | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.651+7017G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271536 | ||||||
| chr1:183271560
|
C | G | 29 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(26): Show | 29 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.651+6993G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271560 | ||||||
| chr1:183271680
|
CG | C | 42 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.651+6872delC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271680 | ||||||
| chr1:183271749
|
T | C | 3 | a0001c0001t0005g0077a0001c0001t0077g0193a0001c0001t0082g0034 | 3 | HG01361.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.651+6804A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271749 | ||||||
| chr1:183271972
|
T | C | 2 | a0001c0001t0035g0031a0001c0001t0035g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.651+6581A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183271972 | ||||||
| chr1:183272043
|
A | G | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.651+6510T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272043 | ||||||
| chr1:183272127
|
G | A | 110 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.651+6426C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272127 | ||||||
| chr1:183272260
|
G | C | 1 | a0001c0001t0092g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.651+6293C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272260 | ||||||
| chr1:183272310
|
T | G | 46 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(43): Show | 46 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.651+6243A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272310 | ||||||
| chr1:183272325
|
T | A | 4 | a0001c0001t0011g0192a0001c0001t0032g0108a0001c0001t0032g0184others(1): Show | 4 | HG01192.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+6228A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272325 | ||||||
| chr1:183272367
|
G | A | 1 | a0001c0001t0012g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.651+6186C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272367 | ||||||
| chr1:183272542
|
T | C | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+6011A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272542 | ||||||
| chr1:183272584
|
G | T | 2 | a0001c0001t0002g0158a0001c0001t0018g0159 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.651+5969C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272584 | ||||||
| chr1:183272592
|
C | A | 3 | a0001c0001t0033g0110a0001c0001t0033g0246a0001c0001t0058g0237 | 3 | HG01891.hp2 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.651+5961G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272592 | ||||||
| chr1:183272601
|
T | A | 8 | a0001c0001t0002g0082a0001c0001t0004g0178a0001c0001t0004g0233others(5): Show | 8 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+5952A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272601 | ||||||
| chr1:183272646
|
G | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.651+5907C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272646 | ||||||
| chr1:183272760
|
C | T | 6 | a0001c0001t0002g0041a0001c0001t0002g0158a0001c0001t0012g0155others(3): Show | 6 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+5793G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272760 | ||||||
| chr1:183272866
|
G | C | 44 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(41): Show | 44 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.651+5687C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183272866 | ||||||
| chr1:183273113
|
A | C | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.651+5440T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273113 | ||||||
| chr1:183273211
|
G | A | 20 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(17): Show | 20 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.651+5342C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273211 | ||||||
| chr1:183273315
|
A | G | 26 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(23): Show | 26 | HG00609.hp1 HG01106.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.651+5238T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273315 | ||||||
| chr1:183273390
|
G | A | 1 | a0001c0001t0004g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.651+5163C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273390 | ||||||
| chr1:183273625
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.651+4928G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273625 | ||||||
| chr1:183273760
|
C | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+4793G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273760 | ||||||
| chr1:183273823
|
T | TTCCC | 8 | a0001c0001t0006g0098a0001c0001t0006g0202a0001c0001t0006g0203others(5): Show | 8 | HG01099.hp1 HG02155.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.651+4726_651+4729d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273823 | ||||||
| chr1:183273823
|
T | TTCCCTCC others(13): Show |
1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.651+4710_651+4729d others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273823 | ||||||
| chr1:183273834
|
CCTCCCTC others(12): Show |
C | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.651+4700_651+4718d others(21): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273834 | ||||||
| chr1:183273835
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.651+4718G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273835 | ||||||
| chr1:183273841
|
C | CCCTCCCT others(9): Show |
1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.651+4711_651+4712i others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTT | C | 7 | a0001c0001t0011g0103a0001c0001t0016g0254a0001c0001t0030g0169others(4): Show | 7 | HG01109.hp2 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+4708_651+4711d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTTCCT others(1): Show |
C | 24 | a0001c0001t0002g0001a0001c0001t0002g0049a0001c0001t0002g0158others(21): Show | 25 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.651+4704_651+4711d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTTCCT others(5): Show |
C | 80 | a0001c0001t0002g0013a0001c0001t0002g0037a0001c0001t0002g0041others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.651+4700_651+4711d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTTCCT others(9): Show |
C | 27 | a0001c0001t0001g0227a0001c0001t0002g0082a0001c0001t0002g0086others(24): Show | 27 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.651+4696_651+4711d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTTCCT others(13): Show |
C | 69 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(66): Show | 69 | HG00609.hp1 HG00738.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.651+4692_651+4711d others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273841
|
CCCTTCCT others(17): Show |
C | 12 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(9): Show | 12 | HG02280.hp2 HG02523.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.651+4688_651+4711d others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273841 | ||||||
| chr1:183273845
|
T | C | 31 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(28): Show | 31 | HG00423.hp2 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.651+4708A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273845 | ||||||
| chr1:183273849
|
T | C | 34 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(31): Show | 34 | HG00423.hp2 HG00735.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.651+4704A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273849 | ||||||
| chr1:183273853
|
T | C | 53 | a0001c0001t0002g0001a0001c0001t0002g0049a0001c0001t0002g0158others(50): Show | 54 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.651+4700A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273853 | ||||||
| chr1:183273856
|
T | C | 1 | a0001c0001t0039g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.651+4697A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273856 | ||||||
| chr1:183273857
|
T | C | 132 | a0001c0001t0001g0228a0001c0001t0002g0001a0001c0001t0002g0013others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.651+4696A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273857 | ||||||
| chr1:183273860
|
T | C | 1 | a0001c0001t0039g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.651+4693A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273860 | ||||||
| chr1:183273861
|
T | C | 144 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0002g0013others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.651+4692A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273861 | ||||||
| chr1:183273865
|
T | C | 125 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(122): Show | 125 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.651+4688A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273865 | ||||||
| chr1:183273869
|
T | C | 55 | a0001c0001t0002g0149a0001c0001t0003g0062a0001c0001t0007g0019others(52): Show | 55 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.651+4684A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273869 | ||||||
| chr1:183273873
|
T | C | 54 | a0001c0001t0002g0149a0001c0001t0007g0019a0001c0001t0007g0020others(51): Show | 54 | HG00609.hp1 HG01069.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.651+4680A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273873 | ||||||
| chr1:183273877
|
T | C | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.651+4676A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273877 | ||||||
| chr1:183273908
|
C | T | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.651+4645G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273908 | ||||||
| chr1:183273954
|
T | C | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.651+4599A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183273954 | ||||||
| chr1:183274080
|
T | C | 26 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(23): Show | 26 | HG00609.hp1 HG01106.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.651+4473A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274080 | ||||||
| chr1:183274121
|
C | T | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.651+4432G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274121 | ||||||
| chr1:183274138
|
C | A | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.651+4415G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274138 | ||||||
| chr1:183274214
|
G | T | 2 | a0001c0001t0030g0017a0001c0001t0057g0249 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.651+4339C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274214 | ||||||
| chr1:183274389
|
G | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+4164C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274389 | ||||||
| chr1:183274405
|
G | A | 6 | a0001c0001t0024g0099a0001c0001t0026g0117a0001c0001t0027g0185others(3): Show | 6 | HG02145.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+4148C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274405 | ||||||
| chr1:183274487
|
A | G | 1 | a0001c0001t0062g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.651+4066T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274487 | ||||||
| chr1:183274766
|
T | TA | 13 | a0001c0001t0003g0163a0001c0001t0004g0006a0001c0001t0004g0054others(10): Show | 13 | HG00140.hp2 HG00738.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.651+3786dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274766 | ||||||
| chr1:183274766
|
TA | T | 5 | a0001c0001t0013g0067a0001c0001t0013g0090a0001c0001t0013g0129others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+3786delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274766 | ||||||
| chr1:183274907
|
T | G | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+3646A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274907 | ||||||
| chr1:183274996
|
A | G | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+3557T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183274996 | ||||||
| chr1:183275000
|
G | A | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+3553C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275000 | ||||||
| chr1:183275518
|
G | A | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.651+3035C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275518 | ||||||
| chr1:183275612
|
G | A | 4 | a0001c0001t0062g0225a0001c0001t0068g0208a0001c0001t0070g0113others(1): Show | 4 | HG02602.hp1 HG03017.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+2941C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275612 | ||||||
| chr1:183275643
|
G | A | 2 | a0001c0001t0005g0239a0001c0001t0009g0084 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.651+2910C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275643 | ||||||
| chr1:183275676
|
A | AT | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.651+2876dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275676 | ||||||
| chr1:183275704
|
G | T | 96 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.651+2849C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275704 | ||||||
| chr1:183275771
|
C | T | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.651+2782G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275771 | ||||||
| chr1:183275923
|
C | T | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.651+2630G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275923 | ||||||
| chr1:183275991
|
G | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+2562C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183275991 | ||||||
| chr1:183276080
|
C | G | 29 | a0001c0001t0006g0007a0001c0001t0006g0061a0001c0001t0006g0097others(26): Show | 29 | HG00423.hp2 HG00735.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.651+2473G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276080 | ||||||
| chr1:183276150
|
C | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.651+2403G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276150 | ||||||
| chr1:183276224
|
A | G | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.651+2329T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276224 | ||||||
| chr1:183276304
|
A | G | 244 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.651+2249T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276304 | ||||||
| chr1:183276362
|
C | A | 1 | a0001c0001t0020g0096 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.651+2191G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276362 | ||||||
| chr1:183276457
|
C | T | 1 | a0001c0001t0072g0010 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.651+2096G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276457 | ||||||
| chr1:183276539
|
G | A | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.651+2014C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276539 | ||||||
| chr1:183276931
|
C | T | 241 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.651+1622G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183276931 | ||||||
| chr1:183277084
|
G | A | 1 | a0001c0001t0009g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.651+1469C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277084 | ||||||
| chr1:183277118
|
C | A | 1 | a0001c0001t0057g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.651+1435G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277118 | ||||||
| chr1:183277206
|
A | T | 5 | a0001c0001t0017g0002a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02280.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.651+1347T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277206 | ||||||
| chr1:183277320
|
T | G | 1 | a0001c0003t0015g0224 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.651+1233A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277320 | ||||||
| chr1:183277343
|
C | T | 3 | a0001c0001t0030g0017a0001c0001t0030g0169a0001c0001t0057g0249 | 3 | HG01099.hp1 HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.651+1210G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277343 | ||||||
| chr1:183277357
|
C | G | 117 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.651+1196G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277357 | ||||||
| chr1:183277398
|
G | A | 117 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0037others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.651+1155C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277398 | ||||||
| chr1:183277464
|
G | C | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.651+1089C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277464 | ||||||
| chr1:183277512
|
C | CA | 16 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0003g0163others(13): Show | 16 | HG00140.hp1 HG01081.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.651+1040dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277512 | ||||||
| chr1:183277512
|
CA | C | 43 | a0001c0001t0001g0101a0001c0001t0001g0139a0001c0001t0003g0062others(40): Show | 43 | HG00423.hp2 HG00735.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.651+1040delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277512 | ||||||
| chr1:183277512
|
CAA | C | 32 | a0001c0001t0002g0082a0001c0001t0002g0149a0001c0001t0006g0098others(29): Show | 32 | HG01069.hp1 HG01099.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.651+1039_651+1040d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277512 | ||||||
| chr1:183277512
|
CAAA | C | 7 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(4): Show | 7 | HG02280.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.651+1038_651+1040d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277512 | ||||||
| chr1:183277531
|
A | G | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.651+1022T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277531 | ||||||
| chr1:183277715
|
A | G | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+838T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277715 | ||||||
| chr1:183277716
|
T | C | 26 | a0001c0001t0002g0149a0001c0001t0010g0009a0001c0001t0010g0011others(23): Show | 26 | HG00609.hp1 HG01106.hp2 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.651+837A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277716 | ||||||
| chr1:183277887
|
G | C | 40 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(37): Show | 40 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.651+666C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277887 | ||||||
| chr1:183277955
|
C | T | 38 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.651+598G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277955 | ||||||
| chr1:183277956
|
G | A | 2 | a0001c0001t0032g0108a0001c0001t0032g0184 | 2 | HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.651+597C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183277956 | ||||||
| chr1:183278042
|
G | A | 4 | a0001c0001t0030g0017a0001c0001t0030g0169a0001c0001t0056g0151others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+511C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278042 | ||||||
| chr1:183278234
|
G | C | 15 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(12): Show | 15 | HG02280.hp2 HG02523.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.651+319C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278234 | ||||||
| chr1:183278280
|
T | C | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.651+273A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278280 | ||||||
| chr1:183278359
|
T | C | 2 | a0001c0001t0033g0110a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.651+194A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278359 | ||||||
| chr1:183278401
|
T | A | 1 | a0001c0001t0053g0180 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.651+152A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278401 | ||||||
| chr1:183278526
|
G | T | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.651+27C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 8/10 | chr1 | 183278526 | ||||||
| chr1:183278763
|
C | T | 6 | a0001c0001t0017g0002a0001c0001t0017g0171a0001c0001t0017g0173others(3): Show | 6 | HG02280.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.575-134G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183278763 | ||||||
| chr1:183278818
|
C | T | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.575-189G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183278818 | ||||||
| chr1:183278973
|
C | T | 1 | a0001c0001t0018g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.575-344G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183278973 | ||||||
| chr1:183279380
|
A | T | 1 | a0001c0001t0047g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.575-751T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183279380 | ||||||
| chr1:183279441
|
C | A | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.575-812G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183279441 | ||||||
| chr1:183279459
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.575-830C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183279459 | ||||||
| chr1:183279515
|
C | T | 1 | a0001c0001t0009g0232 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.575-886G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183279515 | ||||||
| chr1:183280135
|
A | G | 1 | a0001c0001t0028g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.575-1506T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280135 | ||||||
| chr1:183280221
|
G | T | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.575-1592C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280221 | ||||||
| chr1:183280336
|
T | C | 1 | a0001c0001t0003g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.575-1707A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280336 | ||||||
| chr1:183280377
|
GTAA | G | 5 | a0001c0001t0011g0103a0001c0001t0011g0105a0001c0001t0011g0106others(2): Show | 5 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.575-1751_575-1749d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280377 | ||||||
| chr1:183280601
|
A | T | 1 | a0001c0001t0013g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.575-1972T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280601 | ||||||
| chr1:183280603
|
T | G | 1 | a0001c0001t0013g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.575-1974A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280603 | ||||||
| chr1:183280608
|
A | G | 1 | a0001c0001t0013g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.575-1979T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280608 | ||||||
| chr1:183280641
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.575-2012C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280641 | ||||||
| chr1:183280737
|
C | CT | 22 | a0001c0001t0001g0101a0001c0001t0002g0013a0001c0001t0005g0047others(19): Show | 22 | HG00735.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.575-2109dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280737 | ||||||
| chr1:183280775
|
AT | A | 10 | a0001c0001t0004g0006a0001c0001t0005g0077a0001c0001t0030g0017others(7): Show | 10 | HG01109.hp2 HG01123.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.575-2147delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280775 | ||||||
| chr1:183280775
|
ATT | A | 26 | a0001c0001t0002g0210a0001c0001t0006g0007a0001c0001t0006g0202others(23): Show | 26 | HG00423.hp2 HG01099.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.575-2148_575-2147d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280775 | ||||||
| chr1:183280775
|
ATTT | A | 130 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.575-2149_575-2147d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280775 | ||||||
| chr1:183280775
|
ATTTT | A | 66 | a0001c0001t0002g0001a0001c0001t0002g0082a0001c0001t0002g0149others(63): Show | 67 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.575-2150_575-2147d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280775 | ||||||
| chr1:183280775
|
ATTTTT | A | 16 | a0001c0001t0002g0221a0001c0001t0005g0076a0001c0001t0008g0042others(13): Show | 16 | HG01099.hp2 HG01192.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.575-2151_575-2147d others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280775 | ||||||
| chr1:183280994
|
A | G | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.575-2365T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183280994 | ||||||
| chr1:183281028
|
G | A | 39 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.575-2399C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281028 | ||||||
| chr1:183281074
|
C | T | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.575-2445G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281074 | ||||||
| chr1:183281094
|
T | C | 5 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-2465A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281094 | ||||||
| chr1:183281096
|
T | A | 5 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-2467A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281096 | ||||||
| chr1:183281134
|
A | G | 1 | a0001c0001t0002g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.575-2505T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281134 | ||||||
| chr1:183281391
|
T | G | 1 | a0001c0001t0085g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.574+2604A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281391 | ||||||
| chr1:183281562
|
G | A | 1 | a0001c0001t0003g0217 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.574+2433C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281562 | ||||||
| chr1:183281914
|
T | A | 1 | a0001c0001t0088g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.574+2081A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281914 | ||||||
| chr1:183281915
|
C | T | 1 | a0001c0001t0088g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.574+2080G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281915 | ||||||
| chr1:183281919
|
T | C | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.574+2076A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281919 | ||||||
| chr1:183281945
|
G | C | 187 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.574+2050C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183281945 | ||||||
| chr1:183282023
|
G | A | 1 | a0001c0001t0085g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.574+1972C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183282023 | ||||||
| chr1:183282184
|
G | T | 1 | a0001c0001t0047g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.574+1811C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183282184 | ||||||
| chr1:183282305
|
A | G | 1 | a0001c0001t0047g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.574+1690T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183282305 | ||||||
| chr1:183283223
|
G | A | 2 | a0001c0001t0056g0151a0001c0001t0090g0226 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.574+772C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283223 | ||||||
| chr1:183283359
|
C | T | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.574+636G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283359 | ||||||
| chr1:183283475
|
C | T | 1 | a0001c0001t0090g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.574+520G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283475 | ||||||
| chr1:183283476
|
G | A | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574+519C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283476 | ||||||
| chr1:183283523
|
C | T | 2 | a0001c0001t0020g0095a0001c0001t0020g0096 | 2 | NA18946.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.574+472G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283523 | ||||||
| chr1:183283529
|
CACAG | C | 73 | a0001c0001t0001g0035a0001c0001t0002g0001a0001c0001t0002g0149others(70): Show | 74 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.574+462_574+465del others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283529 | ||||||
| chr1:183283582
|
G | T | 5 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.574+413C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283582 | ||||||
| chr1:183283654
|
C | A | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.574+341G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283654 | ||||||
| chr1:183283655
|
T | A | 1 | a0001c0001t0005g0047 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.574+340A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 7/10 | chr1 | 183283655 | ||||||
| chr1:183284078
|
G | A | 58 | a0001c0001t0002g0037a0001c0001t0002g0041a0001c0001t0002g0049others(55): Show | 58 | HG00099.hp1 HG00609.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.530-39C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 6/10 | chr1 | 183284078 | ||||||
| chr1:183284083
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.530-44G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 6/10 | chr1 | 183284083 | ||||||
| chr1:183284299
|
C | T | 2 | a0001c0001t0007g0019a0001c0001t0007g0020 | 2 | NA18950.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.530-260G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 6/10 | chr1 | 183284299 | ||||||
| chr1:183284682
|
C | T | 1 | a0001c0001t0089g0085 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.529+28G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 6/10 | chr1 | 183284682 | ||||||
| chr1:183284824
|
T | C | 2 | a0001c0001t0042g0058a0001c0001t0042g0179 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.449-34A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183284824 | ||||||
| chr1:183284824
|
T | G | 100 | a0001c0001t0002g0013a0001c0001t0002g0037a0001c0001t0002g0041others(97): Show | 100 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.449-34A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183284824 | ||||||
| chr1:183284835
|
A | C | 8 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.449-45T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183284835 | ||||||
| chr1:183285050
|
T | C | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.449-260A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183285050 | ||||||
| chr1:183285353
|
T | C | 245 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.449-563A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183285353 | ||||||
| chr1:183285837
|
C | T | 48 | a0001c0001t0002g0037a0001c0001t0002g0041a0001c0001t0002g0049others(45): Show | 48 | HG00099.hp1 HG00609.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.448+825G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183285837 | ||||||
| chr1:183285932
|
G | A | 153 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.448+730C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183285932 | ||||||
| chr1:183286097
|
G | A | 98 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.448+565C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183286097 | ||||||
| chr1:183286191
|
C | T | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+471G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183286191 | ||||||
| chr1:183286280
|
T | G | 1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.448+382A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183286280 | ||||||
| chr1:183286425
|
A | C | 2 | a0001c0001t0032g0108a0001c0001t0032g0184 | 2 | HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.448+237T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 5/10 | chr1 | 183286425 | ||||||
| chr1:183286836
|
G | A | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.322-48C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183286836 | ||||||
| chr1:183286943
|
G | A | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.322-155C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183286943 | ||||||
| chr1:183286971
|
G | A | 2 | a0001c0001t0006g0202a0001c0001t0006g0203 | 2 | NA18970.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.322-183C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183286971 | ||||||
| chr1:183287046
|
C | T | 3 | a0001c0001t0024g0099a0001c0001t0026g0117a0001c0001t0043g0074 | 3 | HG02717.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.322-258G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183287046 | ||||||
| chr1:183287094
|
C | G | 2 | a0001c0001t0011g0192a0001c0001t0030g0017 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.322-306G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183287094 | ||||||
| chr1:183287321
|
C | T | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322-533G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183287321 | ||||||
| chr1:183287575
|
G | A | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322-787C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183287575 | ||||||
| chr1:183287809
|
G | A | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.322-1021C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183287809 | ||||||
| chr1:183288054
|
G | A | 199 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.322-1266C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288054 | ||||||
| chr1:183288083
|
C | T | 47 | a0001c0001t0002g0037a0001c0001t0002g0041a0001c0001t0002g0049others(44): Show | 47 | HG00099.hp1 HG00609.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.322-1295G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288083 | ||||||
| chr1:183288322
|
C | T | 1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.322-1534G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288322 | ||||||
| chr1:183288343
|
A | C | 192 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.322-1555T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288343 | ||||||
| chr1:183288343
|
A | T | 7 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0037g0252others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-1555T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288343 | ||||||
| chr1:183288344
|
G | A | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.322-1556C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288344 | ||||||
| chr1:183288519
|
C | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | NA18953.hp2 NA18968.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1609G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288519 | ||||||
| chr1:183288703
|
C | G | 1 | a0001c0001t0054g0060 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.321+1425G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288703 | ||||||
| chr1:183288852
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.321+1276C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288852 | ||||||
| chr1:183288966
|
C | T | 5 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1162G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183288966 | ||||||
| chr1:183289023
|
C | A | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.321+1105G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289023 | ||||||
| chr1:183289131
|
C | T | 6 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(3): Show | 6 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+997G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289131 | ||||||
| chr1:183289270
|
T | C | 1 | a0001c0001t0003g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.321+858A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289270 | ||||||
| chr1:183289345
|
T | G | 2 | a0001c0001t0003g0163a0001c0001t0055g0188 | 2 | HG01169.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.321+783A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289345 | ||||||
| chr1:183289538
|
T | C | 16 | a0001c0001t0005g0209a0001c0001t0010g0009a0001c0001t0010g0011others(13): Show | 16 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+590A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289538 | ||||||
| chr1:183289586
|
G | A | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.321+542C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289586 | ||||||
| chr1:183289593
|
T | A | 1 | a0001c0001t0060g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.321+535A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289593 | ||||||
| chr1:183289602
|
G | A | 1 | a0001c0001t0004g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.321+526C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289602 | ||||||
| chr1:183289857
|
C | G | 5 | a0001c0001t0004g0178a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+271G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289857 | ||||||
| chr1:183289933
|
C | T | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.321+195G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289933 | ||||||
| chr1:183289990
|
G | A | 47 | a0001c0001t0002g0001a0001c0001t0002g0164a0001c0001t0002g0221others(44): Show | 48 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.321+138C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183289990 | ||||||
| chr1:183290115
|
T | C | 7 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0004g0251others(4): Show | 7 | HG02717.hp1 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+13A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183290115 | ||||||
| chr1:183290115
|
T | G | 1 | a0001c0001t0012g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.321+13A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 4/10 | chr1 | 183290115 | ||||||
| chr1:183290319
|
G | T | 1 | a0001c0001t0008g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.243-113C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290319 | ||||||
| chr1:183290468
|
T | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0164a0001c0001t0002g0221others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.243-262A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290468 | ||||||
| chr1:183290629
|
T | G | 1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.243-423A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290629 | ||||||
| chr1:183290677
|
A | T | 2 | a0001c0001t0035g0031a0001c0001t0035g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.243-471T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290677 | ||||||
| chr1:183290747
|
C | T | 18 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(15): Show | 18 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.243-541G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290747 | ||||||
| chr1:183290849
|
C | T | 2 | a0001c0001t0027g0185a0001c0001t0027g0235 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.243-643G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290849 | ||||||
| chr1:183290867
|
G | A | 1 | a0001c0001t0005g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.243-661C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183290867 | ||||||
| chr1:183291017
|
A | G | 1 | a0001c0001t0003g0032 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.243-811T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291017 | ||||||
| chr1:183291172
|
C | T | 15 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(12): Show | 15 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.243-966G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291172 | ||||||
| chr1:183291286
|
T | C | 1 | a0001c0001t0004g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.243-1080A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291286 | ||||||
| chr1:183291388
|
C | T | 1 | a0001c0001t0086g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.243-1182G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291388 | ||||||
| chr1:183291524
|
A | G | 19 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0006others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.242+1266T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291524 | ||||||
| chr1:183291650
|
C | G | 2 | a0001c0001t0056g0151a0001c0001t0090g0226 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.242+1140G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291650 | ||||||
| chr1:183291716
|
C | G | 109 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0149others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.242+1074G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291716 | ||||||
| chr1:183291727
|
A | G | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.242+1063T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291727 | ||||||
| chr1:183291759
|
C | T | 37 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0049others(34): Show | 38 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.242+1031G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291759 | ||||||
| chr1:183291921
|
A | G | 8 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.242+869T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183291921 | ||||||
| chr1:183292155
|
G | C | 18 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(15): Show | 18 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.242+635C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183292155 | ||||||
| chr1:183292252
|
A | T | 7 | a0001c0001t0003g0029a0001c0001t0010g0009a0001c0001t0010g0011others(4): Show | 7 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.242+538T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183292252 | ||||||
| chr1:183292575
|
A | G | 152 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.242+215T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 3/10 | chr1 | 183292575 | ||||||
| chr1:183292871
|
G | C | 17 | a0001c0001t0003g0029a0001c0001t0005g0005a0001c0001t0005g0209others(14): Show | 17 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.175-14C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183292871 | ||||||
| chr1:183293046
|
C | A | 1 | a0001c0001t0039g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.175-189G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183293046 | ||||||
| chr1:183293240
|
T | C | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.175-383A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183293240 | ||||||
| chr1:183293434
|
T | C | 143 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.174+271A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183293434 | ||||||
| chr1:183293455
|
C | T | 3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.174+250G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183293455 | ||||||
| chr1:183293501
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.174+204A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 2/10 | chr1 | 183293501 | ||||||
| chr1:183293866
|
C | T | 4 | a0001c0001t0002g0082a0001c0001t0030g0169a0001c0001t0033g0246others(1): Show | 4 | HG01069.hp1 HG01109.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-73G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183293866 | ||||||
| chr1:183294167
|
A | AAAAT | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-378_86-375dupAT others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294167 | ||||||
| chr1:183294213
|
T | C | 2 | a0001c0001t0035g0031a0001c0001t0035g0161 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.86-420A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294213 | ||||||
| chr1:183294221
|
T | G | 83 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0002g0164others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.86-428A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294221 | ||||||
| chr1:183294460
|
G | A | 1 | a0001c0001t0012g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-667C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294460 | ||||||
| chr1:183294494
|
T | C | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-701A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294494 | ||||||
| chr1:183294624
|
T | A | 1 | a0001c0001t0047g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.86-831A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294624 | ||||||
| chr1:183294652
|
C | T | 2 | a0001c0001t0024g0087a0001c0001t0028g0255 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.86-859G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294652 | ||||||
| chr1:183294660
|
G | A | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.86-867C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294660 | ||||||
| chr1:183294662
|
C | T | 12 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0006others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-869G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294662 | ||||||
| chr1:183294745
|
G | A | 1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86-952C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294745 | ||||||
| chr1:183294958
|
T | C | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-1165A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183294958 | ||||||
| chr1:183295093
|
T | A | 11 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-1300A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295093 | ||||||
| chr1:183295208
|
G | T | 19 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0006others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.86-1415C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295208 | ||||||
| chr1:183295317
|
A | G | 2 | a0001c0001t0002g0210a0001c0001t0038g0190 | 2 | HG02523.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.86-1524T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295317 | ||||||
| chr1:183295375
|
G | A | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-1582C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295375 | ||||||
| chr1:183295519
|
T | A | 143 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.86-1726A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295519 | ||||||
| chr1:183295607
|
T | C | 143 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.86-1814A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295607 | ||||||
| chr1:183295700
|
C | T | 3 | a0001c0001t0027g0185a0001c0001t0027g0235a0001c0001t0090g0226 | 3 | HG02145.hp1 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.86-1907G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295700 | ||||||
| chr1:183295714
|
T | A | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-1921A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295714 | ||||||
| chr1:183295771
|
C | G | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-1978G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295771 | ||||||
| chr1:183295889
|
C | T | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-2096G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295889 | ||||||
| chr1:183295909
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2116G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295909 | ||||||
| chr1:183295920
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2127G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295920 | ||||||
| chr1:183295952
|
G | A | 11 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-2159C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295952 | ||||||
| chr1:183295985
|
ATTACAGG others(17): Show |
A | 1 | a0001c0003t0015g0224 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.86-2216_86-2193del others(24): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183295985 | ||||||
| chr1:183296010
|
A | G | 1 | a0001c0003t0015g0224 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.86-2217T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296010 | ||||||
| chr1:183296023
|
T | G | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-2230A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296023 | ||||||
| chr1:183296025
|
T | C | 44 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(41): Show | 44 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.86-2232A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296025 | ||||||
| chr1:183296093
|
G | A | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-2300C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296093 | ||||||
| chr1:183296098
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2305G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296098 | ||||||
| chr1:183296128
|
G | A | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-2335C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296128 | ||||||
| chr1:183296145
|
C | T | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-2352G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296145 | ||||||
| chr1:183296246
|
A | G | 137 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.86-2453T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296246 | ||||||
| chr1:183296271
|
T | C | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-2478A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296271 | ||||||
| chr1:183296310
|
A | G | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2517T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296310 | ||||||
| chr1:183296441
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.86-2648G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296441 | ||||||
| chr1:183296442
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.86-2649A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296442 | ||||||
| chr1:183296505
|
T | C | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.86-2712A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296505 | ||||||
| chr1:183296522
|
C | CT | 11 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-2730dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296522 | ||||||
| chr1:183296522
|
C | CTT | 114 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.86-2731_86-2730dup others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296522 | ||||||
| chr1:183296522
|
C | CTTT | 13 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0006others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.86-2732_86-2730dup others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296522 | ||||||
| chr1:183296535
|
T | C | 157 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.86-2742A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296535 | ||||||
| chr1:183296544
|
G | A | 1 | a0001c0001t0016g0254 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.86-2751C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296544 | ||||||
| chr1:183296575
|
T | C | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2782A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296575 | ||||||
| chr1:183296601
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-2808G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296601 | ||||||
| chr1:183296620
|
C | T | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-2827G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296620 | ||||||
| chr1:183296666
|
C | T | 32 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.86-2873G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296666 | ||||||
| chr1:183296696
|
T | A | 3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-2903A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296696 | ||||||
| chr1:183296712
|
C | T | 3 | a0001c0001t0011g0192a0001c0001t0025g0014a0001c0001t0025g0016 | 3 | HG02055.hp1 HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.86-2919G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296712 | ||||||
| chr1:183296768
|
C | T | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-2975G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296768 | ||||||
| chr1:183296807
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.86-3014G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296807 | ||||||
| chr1:183296845
|
T | C | 2 | a0001c0001t0062g0225a0001c0001t0071g0025 | 2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.86-3052A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296845 | ||||||
| chr1:183296961
|
C | G | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3168G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183296961 | ||||||
| chr1:183297047
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3254G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297047 | ||||||
| chr1:183297110
|
AC | A | 4 | a0001c0001t0002g0082a0001c0001t0030g0169a0001c0001t0033g0246others(1): Show | 4 | HG01069.hp1 HG01109.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-3318delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297110 | ||||||
| chr1:183297143
|
G | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3350C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297143 | ||||||
| chr1:183297258
|
G | C | 19 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(16): Show | 19 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.86-3465C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297258 | ||||||
| chr1:183297311
|
T | G | 1 | a0001c0001t0014g0070 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.86-3518A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297311 | ||||||
| chr1:183297383
|
CT | C | 22 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(19): Show | 22 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.86-3591delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297383 | ||||||
| chr1:183297383
|
CTTT | C | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3593_86-3591del others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297383 | ||||||
| chr1:183297476
|
G | A | 32 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.86-3683C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297476 | ||||||
| chr1:183297484
|
G | A | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.86-3691C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297484 | ||||||
| chr1:183297508
|
G | A | 103 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.86-3715C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297508 | ||||||
| chr1:183297534
|
C | A | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-3741G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297534 | ||||||
| chr1:183297554
|
G | A | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.86-3761C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297554 | ||||||
| chr1:183297596
|
A | G | 157 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.86-3803T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297596 | ||||||
| chr1:183297679
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3886G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297679 | ||||||
| chr1:183297749
|
C | T | 138 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.86-3956G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297749 | ||||||
| chr1:183297874
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.86-4081T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297874 | ||||||
| chr1:183297977
|
G | T | 1 | a0001c0001t0012g0215 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.86-4184C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183297977 | ||||||
| chr1:183298048
|
C | T | 83 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0002g0164others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.86-4255G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298048 | ||||||
| chr1:183298049
|
G | A | 1 | a0001c0001t0008g0133 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.86-4256C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298049 | ||||||
| chr1:183298114
|
T | C | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-4321A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298114 | ||||||
| chr1:183298115
|
T | C | 2 | a0001c0001t0005g0076a0001c0001t0079g0177 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-4322A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298115 | ||||||
| chr1:183298136
|
G | A | 1 | a0001c0001t0053g0180 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.86-4343C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298136 | ||||||
| chr1:183298385
|
T | C | 44 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(41): Show | 44 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.86-4592A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298385 | ||||||
| chr1:183298409
|
A | AAGTGG | 63 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(60): Show | 63 | HG00140.hp1 HG00738.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.86-4617_86-4616ins others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298409 | ||||||
| chr1:183298560
|
A | G | 1 | a0001c0001t0075g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86-4767T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298560 | ||||||
| chr1:183298580
|
G | A | 11 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-4787C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298580 | ||||||
| chr1:183298785
|
C | A | 39 | a0001c0001t0002g0082a0001c0001t0002g0149a0001c0001t0002g0158others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.86-4992G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298785 | ||||||
| chr1:183298799
|
T | C | 39 | a0001c0001t0002g0082a0001c0001t0002g0149a0001c0001t0002g0158others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.86-5006A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298799 | ||||||
| chr1:183298800
|
G | T | 39 | a0001c0001t0002g0082a0001c0001t0002g0149a0001c0001t0002g0158others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.86-5007C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298800 | ||||||
| chr1:183298906
|
T | A | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-5113A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298906 | ||||||
| chr1:183298992
|
G | A | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-5199C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183298992 | ||||||
| chr1:183299101
|
G | A | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-5308C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299101 | ||||||
| chr1:183299126
|
C | A | 44 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(41): Show | 44 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.86-5333G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299126 | ||||||
| chr1:183299132
|
G | A | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-5339C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299132 | ||||||
| chr1:183299187
|
C | T | 40 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0049others(37): Show | 41 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.86-5394G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299187 | ||||||
| chr1:183299201
|
G | A | 19 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(16): Show | 19 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.86-5408C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299201 | ||||||
| chr1:183299331
|
G | A | 47 | a0001c0001t0002g0164a0001c0001t0002g0221a0001c0001t0002g0222others(44): Show | 47 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-5538C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299331 | ||||||
| chr1:183299335
|
C | T | 2 | a0001c0001t0018g0167a0001c0001t0037g0068 | 2 | HG00280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.86-5542G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299335 | ||||||
| chr1:183299348
|
C | T | 32 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(29): Show | 32 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.86-5555G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299348 | ||||||
| chr1:183299547
|
C | T | 2 | a0001c0001t0009g0084a0001c0001t0017g0002 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.86-5754G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299547 | ||||||
| chr1:183299632
|
A | G | 1 | a0001c0001t0092g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.86-5839T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299632 | ||||||
| chr1:183299652
|
T | TA | 21 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0178others(18): Show | 21 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.86-5860dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299652 | ||||||
| chr1:183299652
|
TA | T | 5 | a0001c0001t0002g0082a0001c0001t0002g0221a0001c0001t0003g0065others(2): Show | 5 | HG01515.hp1 HG02273.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-5860delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299652 | ||||||
| chr1:183299725
|
G | A | 1 | a0001c0001t0029g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.86-5932C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299725 | ||||||
| chr1:183299838
|
A | G | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.86-6045T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299838 | ||||||
| chr1:183299844
|
A | G | 1 | a0001c0001t0009g0232 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.86-6051T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299844 | ||||||
| chr1:183299887
|
G | A | 4 | a0001c0001t0002g0199a0001c0001t0009g0220a0001c0001t0012g0059others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-6094C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183299887 | ||||||
| chr1:183300025
|
A | G | 163 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.86-6232T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300025 | ||||||
| chr1:183300083
|
C | T | 12 | a0001c0001t0003g0029a0001c0001t0005g0005a0001c0001t0005g0209others(9): Show | 12 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-6290G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300083 | ||||||
| chr1:183300135
|
G | A | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-6342C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300135 | ||||||
| chr1:183300172
|
GGTGGGCG others(6): Show |
G | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-6392_86-6380del others(13): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300172 | ||||||
| chr1:183300204
|
C | G | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.86-6411G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300204 | ||||||
| chr1:183300376
|
T | G | 88 | a0001c0001t0002g0086a0001c0001t0002g0149a0001c0001t0002g0153others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.86-6583A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300376 | ||||||
| chr1:183300417
|
G | GA | 91 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0041others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.86-6625dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300417 | ||||||
| chr1:183300418
|
A | G | 28 | a0001c0001t0002g0082a0001c0001t0002g0158a0001c0001t0003g0156others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-6625T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300418 | ||||||
| chr1:183300525
|
G | A | 19 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0006others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.86-6732C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300525 | ||||||
| chr1:183300708
|
A | G | 1 | a0001c0001t0012g0215 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.86-6915T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300708 | ||||||
| chr1:183300766
|
C | A | 8 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-6973G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300766 | ||||||
| chr1:183300806
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.86-7013A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300806 | ||||||
| chr1:183300941
|
T | G | 4 | a0001c0001t0011g0015a0001c0001t0011g0192a0001c0001t0025g0014others(1): Show | 4 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-7148A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300941 | ||||||
| chr1:183300955
|
C | G | 48 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0132others(45): Show | 49 | HG00099.hp1 HG00423.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.86-7162G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183300955 | ||||||
| chr1:183301208
|
A | G | 3 | a0001c0001t0022g0240a0001c0001t0028g0218a0001c0001t0028g0255 | 3 | HG02622.hp1 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.86-7415T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301208 | ||||||
| chr1:183301318
|
C | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-7525G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301318 | ||||||
| chr1:183301603
|
G | A | 186 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.86-7810C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301603 | ||||||
| chr1:183301641
|
G | C | 1 | a0001c0001t0005g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-7848C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301641 | ||||||
| chr1:183301662
|
G | T | 57 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.86-7869C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301662 | ||||||
| chr1:183301692
|
T | G | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-7899A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301692 | ||||||
| chr1:183301699
|
C | T | 1 | a0001c0001t0003g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.86-7906G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183301699 | ||||||
| chr1:183302019
|
T | C | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.86-8226A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302019 | ||||||
| chr1:183302050
|
G | A | 9 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-8257C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302050 | ||||||
| chr1:183302401
|
A | C | 59 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.86-8608T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302401 | ||||||
| chr1:183302437
|
A | C | 1 | a0001c0001t0071g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.86-8644T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302437 | ||||||
| chr1:183302465
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0057 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.86-8672T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302465 | ||||||
| chr1:183302526
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.86-8733G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302526 | ||||||
| chr1:183302694
|
C | A | 1 | a0001c0001t0003g0030 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.86-8901G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302694 | ||||||
| chr1:183302854
|
G | A | 1 | a0001c0001t0078g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.86-9061C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302854 | ||||||
| chr1:183302913
|
G | A | 21 | a0001c0001t0002g0082a0001c0001t0004g0006a0001c0001t0004g0178others(18): Show | 21 | HG00423.hp2 HG01081.hp2 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.86-9120C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302913 | ||||||
| chr1:183302930
|
C | T | 11 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0032g0108others(8): Show | 11 | HG01099.hp1 HG01123.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-9137G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183302930 | ||||||
| chr1:183303034
|
CAGAA | C | 27 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0003g0029others(24): Show | 27 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.86-9245_86-9242del others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303034 | ||||||
| chr1:183303160
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0082others(61): Show | 65 | HG00099.hp1 HG00423.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.86-9367A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303160 | ||||||
| chr1:183303301
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.86-9508G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303301 | ||||||
| chr1:183303351
|
C | T | 59 | a0001c0001t0002g0049a0001c0001t0002g0221a0001c0001t0002g0222others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.86-9558G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303351 | ||||||
| chr1:183303425
|
T | C | 7 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(4): Show | 7 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-9632A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303425 | ||||||
| chr1:183303522
|
T | C | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.86-9729A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303522 | ||||||
| chr1:183303551
|
A | G | 2 | a0001c0001t0006g0202a0001c0001t0006g0203 | 2 | NA18970.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.86-9758T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183303551 | ||||||
| chr1:183304030
|
C | T | 1 | a0001c0001t0027g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.86-10237G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183304030 | ||||||
| chr1:183304213
|
G | A | 2 | a0001c0001t0004g0211a0001c0001t0006g0229 | 2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.86-10420C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183304213 | ||||||
| chr1:183304302
|
G | T | 1 | a0001c0001t0029g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.86-10509C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183304302 | ||||||
| chr1:183304616
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-10823G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183304616 | ||||||
| chr1:183304972
|
G | A | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.86-11179C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183304972 | ||||||
| chr1:183305104
|
C | G | 17 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(14): Show | 17 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.86-11311G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305104 | ||||||
| chr1:183305105
|
C | CT | 41 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(38): Show | 41 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.86-11313dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305105 | ||||||
| chr1:183305227
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.86-11434C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305227 | ||||||
| chr1:183305296
|
G | A | 2 | a0001c0001t0030g0017a0001c0001t0066g0116 | 2 | HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.86-11503C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305296 | ||||||
| chr1:183305332
|
G | A | 1 | a0001c0001t0069g0008 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.86-11539C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305332 | ||||||
| chr1:183305456
|
T | G | 1 | a0001c0001t0046g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-11663A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305456 | ||||||
| chr1:183305504
|
G | A | 1 | a0001c0001t0045g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.86-11711C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305504 | ||||||
| chr1:183305716
|
C | CT | 26 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0003g0029others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.86-11924dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305716
|
C | CTT | 56 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(53): Show | 56 | HG00140.hp1 HG00738.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.86-11925_86-11924d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305716
|
C | CTTT | 56 | a0001c0001t0001g0136a0001c0001t0001g0245a0001c0001t0002g0001others(53): Show | 57 | HG00099.hp1 HG00423.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.86-11926_86-11924d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305716
|
CT | C | 58 | a0001c0001t0002g0149a0001c0001t0003g0030a0001c0001t0003g0032others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-11924delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305716
|
CTT | C | 7 | a0001c0001t0002g0049a0001c0001t0020g0096a0001c0001t0032g0108others(4): Show | 7 | HG01070.hp1 HG01123.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-11925_86-11924d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305716
|
CTTT | C | 5 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0037g0252others(2): Show | 5 | HG02451.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-11926_86-11924d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305716 | ||||||
| chr1:183305795
|
A | G | 1 | a0001c0001t0027g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.86-12002T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305795 | ||||||
| chr1:183305831
|
C | T | 7 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-12038G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305831 | ||||||
| chr1:183305975
|
G | A | 46 | a0001c0001t0002g0001a0001c0001t0002g0037a0001c0001t0002g0164others(43): Show | 47 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.86-12182C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183305975 | ||||||
| chr1:183306012
|
G | A | 36 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(33): Show | 36 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.86-12219C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306012 | ||||||
| chr1:183306133
|
A | T | 7 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-12340T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306133 | ||||||
| chr1:183306174
|
AC | A | 136 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0001others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.86-12382delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306174 | ||||||
| chr1:183306185
|
C | T | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-12392G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306185 | ||||||
| chr1:183306809
|
G | T | 7 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(4): Show | 7 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-13016C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306809 | ||||||
| chr1:183306872
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.86-13079G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306872 | ||||||
| chr1:183306955
|
G | A | 11 | a0001c0001t0002g0153a0001c0001t0003g0029a0001c0001t0005g0005others(8): Show | 11 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-13162C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183306955 | ||||||
| chr1:183307055
|
GA | G | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG02523.hp1 HG03209.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-13263delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307055 | ||||||
| chr1:183307237
|
G | A | 7 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(4): Show | 7 | HG02523.hp1 NA18946.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-13444C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307237 | ||||||
| chr1:183307307
|
CT | C | 64 | a0001c0001t0002g0049a0001c0001t0002g0199a0001c0001t0003g0030others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.86-13515delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307307 | ||||||
| chr1:183307318
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.86-13525A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307318 | ||||||
| chr1:183307449
|
AT | A | 187 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(184): Show | 187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.86-13657delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307449 | ||||||
| chr1:183307451
|
T | A | 1 | a0001c0001t0024g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.86-13658A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307451 | ||||||
| chr1:183307452
|
T | A | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-13659A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307452 | ||||||
| chr1:183307658
|
G | A | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-13865C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307658 | ||||||
| chr1:183307768
|
G | T | 17 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(14): Show | 17 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.86-13975C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307768 | ||||||
| chr1:183307794
|
C | G | 4 | a0001c0001t0032g0108a0001c0001t0032g0184a0001c0001t0033g0110others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-14001G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307794 | ||||||
| chr1:183307871
|
C | T | 8 | a0001c0001t0002g0199a0001c0001t0016g0175a0001c0001t0016g0194others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-14078G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307871 | ||||||
| chr1:183307946
|
G | A | 37 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(34): Show | 37 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.86-14153C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307946 | ||||||
| chr1:183307972
|
C | T | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.86-14179G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183307972 | ||||||
| chr1:183308149
|
A | G | 1 | a0001c0001t0008g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.86-14356T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308149 | ||||||
| chr1:183308267
|
G | A | 2 | a0001c0001t0006g0007a0001c0001t0069g0008 | 2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.86-14474C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308267 | ||||||
| chr1:183308479
|
C | T | 1 | a0001c0001t0090g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86-14686G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308479 | ||||||
| chr1:183308529
|
C | T | 1 | a0001c0001t0015g0040 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.86-14736G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308529 | ||||||
| chr1:183308530
|
G | A | 5 | a0001c0001t0002g0158a0001c0001t0004g0154a0001c0001t0012g0155others(2): Show | 5 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-14737C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308530 | ||||||
| chr1:183308579
|
C | T | 4 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0023g0147others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-14786G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308579 | ||||||
| chr1:183308676
|
A | G | 1 | a0001c0001t0027g0235 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.86-14883T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308676 | ||||||
| chr1:183308764
|
A | G | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-14971T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308764 | ||||||
| chr1:183308860
|
G | A | 7 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-15067C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308860 | ||||||
| chr1:183308939
|
C | T | 1 | a0001c0001t0058g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86-15146G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183308939 | ||||||
| chr1:183309041
|
C | T | 1 | a0001c0001t0058g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.86-15248G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309041 | ||||||
| chr1:183309350
|
G | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-15557C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309350 | ||||||
| chr1:183309359
|
C | T | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.86-15566G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309359 | ||||||
| chr1:183309418
|
C | A | 85 | a0001c0001t0002g0049a0001c0001t0002g0086a0001c0001t0002g0149others(82): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.86-15625G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309418 | ||||||
| chr1:183309547
|
G | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-15754C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309547 | ||||||
| chr1:183309612
|
C | A | 4 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0037g0252others(1): Show | 4 | HG02809.hp2 HG02818.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-15819G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309612 | ||||||
| chr1:183309711
|
A | G | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-15918T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309711 | ||||||
| chr1:183309733
|
C | G | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-15940G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309733 | ||||||
| chr1:183309894
|
G | T | 85 | a0001c0001t0002g0049a0001c0001t0002g0086a0001c0001t0002g0149others(82): Show | 85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.86-16101C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309894 | ||||||
| chr1:183309907
|
T | C | 1 | a0001c0001t0042g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.86-16114A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183309907 | ||||||
| chr1:183310190
|
A | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-16397T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310190 | ||||||
| chr1:183310449
|
G | C | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.86-16656C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310449 | ||||||
| chr1:183310767
|
A | T | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-16974T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310767 | ||||||
| chr1:183310777
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(55): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-16984G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310777 | ||||||
| chr1:183310848
|
G | GA | 59 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(56): Show | 59 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.86-17056dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310848 | ||||||
| chr1:183310848
|
GA | G | 12 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0233others(9): Show | 12 | HG01123.hp2 HG01192.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-17056delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310848 | ||||||
| chr1:183310866
|
G | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-17073C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310866 | ||||||
| chr1:183310964
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.86-17171G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310964 | ||||||
| chr1:183310994
|
C | T | 1 | a0001c0001t0010g0009 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.86-17201G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183310994 | ||||||
| chr1:183311047
|
A | G | 1 | a0001c0001t0003g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.86-17254T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311047 | ||||||
| chr1:183311074
|
G | A | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-17281C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311074 | ||||||
| chr1:183311271
|
C | T | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.86-17478G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311271 | ||||||
| chr1:183311712
|
G | A | 3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-17919C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311712 | ||||||
| chr1:183311722
|
T | TAC | 5 | a0001c0001t0002g0001a0001c0001t0003g0187a0001c0001t0003g0201others(2): Show | 6 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-17931_86-17930d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TAC | T | 43 | a0001c0001t0002g0199a0001c0001t0002g0250a0001c0001t0003g0030others(40): Show | 43 | HG00140.hp2 HG00735.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.86-17931_86-17930d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACAC | T | 38 | a0001c0001t0002g0086a0001c0001t0003g0046a0001c0001t0003g0160others(35): Show | 38 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.86-17933_86-17930d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACAC | T | 55 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(52): Show | 55 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.86-17935_86-17930d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACACA others(1): Show |
T | 6 | a0001c0001t0001g0142a0001c0001t0021g0083a0001c0001t0022g0240others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-17937_86-17930d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0011g0103a0001c0001t0074g0102 | 2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.86-17939_86-17930d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0002g0041a0001c0001t0004g0178a0001c0001t0007g0183others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-17941_86-17930d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACACA others(7): Show |
T | 72 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.86-17943_86-17930d others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311722
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0004g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.86-17945_86-17930d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311722 | ||||||
| chr1:183311738
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0004g0178 | 2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.86-17945G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311738 | ||||||
| chr1:183311740
|
C | T | 46 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(43): Show | 46 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.86-17947G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311740 | ||||||
| chr1:183311825
|
A | G | 89 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-18032T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311825 | ||||||
| chr1:183311864
|
G | A | 25 | a0001c0001t0002g0082a0001c0001t0002g0149a0001c0001t0002g0199others(22): Show | 25 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.86-18071C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311864 | ||||||
| chr1:183311996
|
T | A | 7 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(4): Show | 7 | HG02109.hp2 HG02559.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-18203A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183311996 | ||||||
| chr1:183312155
|
T | C | 2 | a0001c0001t0005g0239a0001c0001t0067g0123 | 2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.86-18362A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312155 | ||||||
| chr1:183312265
|
C | CT | 10 | a0001c0001t0001g0101a0001c0001t0007g0019a0001c0001t0007g0020others(7): Show | 10 | HG00423.hp1 HG03942.hp2 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.86-18473dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312265 | ||||||
| chr1:183312265
|
CT | C | 5 | a0001c0001t0002g0210a0001c0001t0008g0121a0001c0001t0030g0169others(2): Show | 5 | HG01109.hp2 HG01516.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-18473delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312265 | ||||||
| chr1:183312377
|
G | A | 9 | a0001c0001t0002g0153a0001c0001t0003g0029a0001c0001t0010g0026others(6): Show | 9 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-18584C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312377 | ||||||
| chr1:183312508
|
C | T | 17 | a0001c0001t0002g0153a0001c0001t0003g0029a0001c0001t0005g0104others(14): Show | 17 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.86-18715G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312508 | ||||||
| chr1:183312516
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.86-18723T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312516 | ||||||
| chr1:183312537
|
A | G | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-18744T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312537 | ||||||
| chr1:183312569
|
T | TA | 11 | a0001c0001t0002g0149a0001c0001t0004g0233a0001c0001t0004g0236others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-18777dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312569 | ||||||
| chr1:183312569
|
TA | T | 139 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0227others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.86-18777delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312569 | ||||||
| chr1:183312784
|
G | A | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-18991C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183312784 | ||||||
| chr1:183313033
|
G | A | 4 | a0001c0001t0032g0108a0001c0001t0032g0184a0001c0001t0033g0110others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-19240C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313033 | ||||||
| chr1:183313061
|
T | C | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-19268A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313061 | ||||||
| chr1:183313117
|
C | T | 1 | a0001c0001t0002g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.86-19324G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313117 | ||||||
| chr1:183313122
|
G | A | 11 | a0001c0001t0002g0149a0001c0001t0004g0233a0001c0001t0004g0236others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-19329C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313122 | ||||||
| chr1:183313172
|
T | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0228a0001c0001t0009g0120others(4): Show | 7 | HG00735.hp2 HG02074.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-19379A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313172 | ||||||
| chr1:183313316
|
G | A | 1 | a0001c0001t0009g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.86-19523C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313316 | ||||||
| chr1:183313440
|
A | G | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(71): Show | 74 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.86-19647T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313440 | ||||||
| chr1:183313510
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.86-19717G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313510 | ||||||
| chr1:183313538
|
GGTGCAA | G | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-19751_86-19746d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313538 | ||||||
| chr1:183313561
|
C | A | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-19768G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313561 | ||||||
| chr1:183313963
|
T | C | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-20170A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183313963 | ||||||
| chr1:183314665
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.86-20872C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183314665 | ||||||
| chr1:183314775
|
A | G | 1 | a0001c0001t0065g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.86-20982T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183314775 | ||||||
| chr1:183314815
|
A | G | 200 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(197): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.86-21022T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183314815 | ||||||
| chr1:183314834
|
G | A | 72 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.86-21041C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183314834 | ||||||
| chr1:183315095
|
C | T | 22 | a0001c0001t0001g0035a0001c0001t0001g0227a0001c0001t0002g0013others(19): Show | 22 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.86-21302G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315095 | ||||||
| chr1:183315168
|
A | G | 11 | a0001c0001t0002g0149a0001c0001t0004g0233a0001c0001t0004g0236others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-21375T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315168 | ||||||
| chr1:183315392
|
A | G | 1 | a0001c0001t0007g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.86-21599T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315392 | ||||||
| chr1:183315394
|
CAT | C | 35 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0228others(32): Show | 35 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.86-21603_86-21602d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315394 | ||||||
| chr1:183315464
|
T | TTG | 42 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(39): Show | 42 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.86-21673_86-21672d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315464 | ||||||
| chr1:183315672
|
C | T | 1 | a0001c0001t0012g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.86-21879G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315672 | ||||||
| chr1:183315778
|
T | TA | 177 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.86-21986dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315778 | ||||||
| chr1:183315778
|
T | TAA | 7 | a0001c0001t0001g0136a0001c0001t0002g0149a0001c0001t0005g0047others(4): Show | 7 | HG02109.hp1 HG02109.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-21987_86-21986d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315778 | ||||||
| chr1:183315778
|
T | TAAA | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18983.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-21988_86-21986d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315778 | ||||||
| chr1:183315852
|
C | T | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-22059G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315852 | ||||||
| chr1:183315868
|
A | T | 8 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0152others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-22075T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315868 | ||||||
| chr1:183315988
|
T | C | 1 | a0001c0001t0009g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.86-22195A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315988 | ||||||
| chr1:183315989
|
G | T | 2 | a0001c0001t0001g0137a0001c0001t0027g0185 | 2 | HG02145.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.86-22196C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183315989 | ||||||
| chr1:183316138
|
CTTGGGA | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-22351_86-22346d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316138 | ||||||
| chr1:183316275
|
A | G | 24 | a0001c0001t0002g0086a0001c0001t0002g0149a0001c0001t0002g0250others(21): Show | 24 | HG01123.hp2 HG01192.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.86-22482T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316275 | ||||||
| chr1:183316418
|
G | A | 1 | a0001c0001t0014g0073 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.86-22625C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316418 | ||||||
| chr1:183316452
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.86-22659G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316452 | ||||||
| chr1:183316509
|
C | T | 1 | a0001c0001t0055g0188 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.86-22716G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316509 | ||||||
| chr1:183316650
|
G | A | 1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86-22857C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316650 | ||||||
| chr1:183316881
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.86-23088C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316881 | ||||||
| chr1:183316985
|
C | G | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-23192G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183316985 | ||||||
| chr1:183317111
|
T | A | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.86-23318A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317111 | ||||||
| chr1:183317226
|
T | C | 1 | a0001c0001t0031g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.86-23433A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317226 | ||||||
| chr1:183317444
|
G | T | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-23651C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317444 | ||||||
| chr1:183317446
|
G | T | 104 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(101): Show | 104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.86-23653C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317446 | ||||||
| chr1:183317473
|
T | C | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.86-23680A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317473 | ||||||
| chr1:183317495
|
C | G | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-23702G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317495 | ||||||
| chr1:183317635
|
C | T | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.86-23842G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317635 | ||||||
| chr1:183317642
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-23849C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317642 | ||||||
| chr1:183317685
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0132 | 2 | HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.86-23892G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183317685 | ||||||
| chr1:183318044
|
G | C | 9 | a0001c0001t0002g0149a0001c0001t0021g0083a0001c0001t0021g0145others(6): Show | 9 | HG01109.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-24251C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318044 | ||||||
| chr1:183318049
|
A | G | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-24256T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318049 | ||||||
| chr1:183318299
|
C | A | 1 | a0001c0001t0032g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.86-24506G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318299 | ||||||
| chr1:183318470
|
G | T | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.86-24677C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318470 | ||||||
| chr1:183318544
|
C | T | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.86-24751G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318544 | ||||||
| chr1:183318685
|
G | A | 2 | a0001c0001t0009g0084a0001c0001t0017g0002 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.86-24892C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318685 | ||||||
| chr1:183318933
|
G | A | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.86-25140C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318933 | ||||||
| chr1:183318942
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.86-25149T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318942 | ||||||
| chr1:183318943
|
T | C | 1 | a0001c0001t0016g0194 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.86-25150A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183318943 | ||||||
| chr1:183319084
|
C | G | 1 | a0001c0001t0012g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.86-25291G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319084 | ||||||
| chr1:183319312
|
C | T | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-25519G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319312 | ||||||
| chr1:183319322
|
A | T | 1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.86-25529T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319322 | ||||||
| chr1:183319391
|
G | A | 1 | a0001c0001t0087g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.86-25598C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319391 | ||||||
| chr1:183319456
|
G | A | 5 | a0001c0001t0003g0030a0001c0001t0005g0076a0001c0001t0008g0042others(2): Show | 5 | HG01258.hp1 HG02486.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-25663C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319456 | ||||||
| chr1:183319458
|
G | A | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.86-25665C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319458 | ||||||
| chr1:183319696
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-25903A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319696 | ||||||
| chr1:183319717
|
T | A | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-25924A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319717 | ||||||
| chr1:183319885
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.86-26092G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319885 | ||||||
| chr1:183319892
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.86-26099C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319892 | ||||||
| chr1:183319932
|
A | G | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.86-26139T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319932 | ||||||
| chr1:183319940
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-26147G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183319940 | ||||||
| chr1:183320193
|
G | T | 1 | a0001c0001t0019g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.86-26400C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320193 | ||||||
| chr1:183320388
|
G | A | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-26595C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320388 | ||||||
| chr1:183320419
|
C | T | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-26626G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320419 | ||||||
| chr1:183320498
|
C | T | 12 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0251others(9): Show | 12 | HG01123.hp2 HG01192.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-26705G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320498 | ||||||
| chr1:183320509
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0013g0129 | 2 | NA18947.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.86-26716C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320509 | ||||||
| chr1:183320575
|
C | T | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-26782G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320575 | ||||||
| chr1:183320744
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-26951C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320744 | ||||||
| chr1:183320915
|
C | T | 192 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.86-27122G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183320915 | ||||||
| chr1:183321010
|
G | A | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(98): Show | 101 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.86-27217C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321010 | ||||||
| chr1:183321059
|
T | G | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-27266A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321059 | ||||||
| chr1:183321066
|
A | G | 1 | a0001c0001t0013g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.86-27273T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321066 | ||||||
| chr1:183321512
|
A | G | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-27719T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321512 | ||||||
| chr1:183321556
|
A | T | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-27763T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321556 | ||||||
| chr1:183321606
|
G | A | 1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.86-27813C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321606 | ||||||
| chr1:183321635
|
C | G | 1 | a0001c0001t0078g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.86-27842G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321635 | ||||||
| chr1:183321665
|
C | T | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-27872G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321665 | ||||||
| chr1:183321748
|
A | C | 8 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-27955T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183321748 | ||||||
| chr1:183322328
|
G | A | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-28535C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183322328 | ||||||
| chr1:183322655
|
A | G | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-28862T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183322655 | ||||||
| chr1:183322672
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0039g0050 | 2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.86-28879C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183322672 | ||||||
| chr1:183322992
|
C | T | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.86-29199G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183322992 | ||||||
| chr1:183323152
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.86-29359C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323152 | ||||||
| chr1:183323156
|
T | G | 70 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.86-29363A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323156 | ||||||
| chr1:183323175
|
A | G | 3 | a0001c0001t0005g0239a0001c0001t0009g0084a0001c0001t0017g0002 | 3 | HG02280.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.86-29382T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323175 | ||||||
| chr1:183323185
|
G | C | 1 | a0001c0001t0001g0045 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.86-29392C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323185 | ||||||
| chr1:183323212
|
G | A | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.86-29419C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323212 | ||||||
| chr1:183323355
|
T | C | 70 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.86-29562A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323355 | ||||||
| chr1:183323363
|
C | T | 2 | a0001c0001t0002g0158a0001c0001t0018g0159 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.86-29570G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323363 | ||||||
| chr1:183323381
|
A | C | 1 | a0001c0001t0006g0195 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.86-29588T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323381 | ||||||
| chr1:183323520
|
T | G | 1 | a0001c0001t0006g0098 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.86-29727A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323520 | ||||||
| chr1:183323557
|
G | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-29764C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323557 | ||||||
| chr1:183323807
|
C | A | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.86-30014G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323807 | ||||||
| chr1:183323807
|
C | G | 2 | a0001c0001t0056g0151a0001c0001t0090g0226 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.86-30014G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183323807 | ||||||
| chr1:183324132
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-30339A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183324132 | ||||||
| chr1:183324205
|
A | G | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.86-30412T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183324205 | ||||||
| chr1:183324572
|
A | G | 108 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-30779T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183324572 | ||||||
| chr1:183324933
|
T | A | 1 | a0001c0001t0018g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.86-31140A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183324933 | ||||||
| chr1:183325024
|
C | T | 4 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0023g0147others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-31231G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325024 | ||||||
| chr1:183325074
|
A | G | 1 | a0001c0001t0006g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.86-31281T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325074 | ||||||
| chr1:183325281
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-31488A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325281 | ||||||
| chr1:183325295
|
C | G | 108 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-31502G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325295 | ||||||
| chr1:183325304
|
A | G | 2 | a0001c0001t0056g0151a0001c0001t0090g0226 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.86-31511T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325304 | ||||||
| chr1:183325583
|
A | G | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-31790T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325583 | ||||||
| chr1:183325755
|
T | G | 26 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(23): Show | 26 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.86-31962A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325755 | ||||||
| chr1:183325792
|
C | T | 1 | a0001c0001t0035g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.86-31999G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325792 | ||||||
| chr1:183325819
|
G | A | 4 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0023g0147others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-32026C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325819 | ||||||
| chr1:183325934
|
G | T | 24 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(21): Show | 24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.86-32141C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183325934 | ||||||
| chr1:183326062
|
C | A | 5 | a0001c0001t0002g0037a0001c0001t0002g0164a0001c0001t0003g0187others(2): Show | 5 | HG00099.hp1 HG01516.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-32269G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326062 | ||||||
| chr1:183326141
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-32348G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326141 | ||||||
| chr1:183326193
|
T | C | 2 | a0001c0001t0056g0151a0001c0001t0090g0226 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.86-32400A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326193 | ||||||
| chr1:183326375
|
CA | C | 60 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(57): Show | 61 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.86-32583delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326375 | ||||||
| chr1:183326375
|
CAA | C | 13 | a0001c0001t0003g0213a0001c0001t0004g0138a0001c0001t0004g0233others(10): Show | 13 | HG00735.hp1 HG01257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.86-32584_86-32583d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326375 | ||||||
| chr1:183326375
|
CAAA | C | 65 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0124others(62): Show | 65 | HG00140.hp1 HG00738.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.86-32585_86-32583d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326375 | ||||||
| chr1:183326375
|
CAAAA | C | 91 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0125others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.86-32586_86-32583d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326375 | ||||||
| chr1:183326375
|
CAAAAA | C | 6 | a0001c0001t0005g0047a0001c0001t0005g0077a0001c0001t0005g0207others(3): Show | 6 | HG01081.hp2 HG01261.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-32587_86-32583d others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326375 | ||||||
| chr1:183326689
|
A | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-32896T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326689 | ||||||
| chr1:183326795
|
A | G | 108 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-33002T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183326795 | ||||||
| chr1:183327026
|
T | TTATG | 71 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.86-33237_86-33234d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327026 | ||||||
| chr1:183327026
|
T | TTATGTAT others(1): Show |
13 | a0001c0001t0003g0217a0001c0001t0005g0104a0001c0001t0005g0112others(10): Show | 13 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.86-33241_86-33234d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327026 | ||||||
| chr1:183327026
|
T | TTATGTAT others(5): Show |
3 | a0001c0001t0007g0183a0001c0001t0016g0175a0001c0001t0026g0004 | 3 | HG03041.hp1 NA19000.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-33245_86-33234d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327026 | ||||||
| chr1:183327026
|
T | TTATGTAT others(9): Show |
1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.86-33249_86-33234d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327026 | ||||||
| chr1:183327026
|
TTATGTAT others(5): Show |
T | 1 | a0001c0001t0005g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-33245_86-33234d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327026 | ||||||
| chr1:183327058
|
G | GTATGTAT others(5): Show |
4 | a0001c0001t0001g0035a0001c0001t0004g0044a0001c0001t0021g0083others(1): Show | 4 | HG03139.hp2 NA19082.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-33266_86-33265i others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327058 | ||||||
| chr1:183327058
|
G | GTATGTAT others(1): Show |
14 | a0001c0001t0002g0149a0001c0001t0003g0062a0001c0001t0004g0054others(11): Show | 14 | HG00140.hp2 HG02015.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.86-33266_86-33265i others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327058 | ||||||
| chr1:183327058
|
G | GTATT | 89 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0227others(86): Show | 89 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-33269_86-33266d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327058 | ||||||
| chr1:183327135
|
C | T | 108 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(105): Show | 108 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-33342G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327135 | ||||||
| chr1:183327412
|
T | G | 1 | a0001c0001t0075g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86-33619A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327412 | ||||||
| chr1:183327472
|
A | C | 4 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0023g0147others(1): Show | 4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-33679T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327472 | ||||||
| chr1:183327520
|
T | A | 7 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0251others(4): Show | 7 | HG02451.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-33727A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327520 | ||||||
| chr1:183327872
|
G | A | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-34079C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327872 | ||||||
| chr1:183327926
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-34133G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183327926 | ||||||
| chr1:183328154
|
A | G | 8 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-34361T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328154 | ||||||
| chr1:183328233
|
G | C | 1 | a0001c0001t0040g0205 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.86-34440C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328233 | ||||||
| chr1:183328287
|
C | T | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-34494G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328287 | ||||||
| chr1:183328341
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-34548C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328341 | ||||||
| chr1:183328419
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.86-34626C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328419 | ||||||
| chr1:183328478
|
A | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-34685T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328478 | ||||||
| chr1:183328691
|
A | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-34898T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328691 | ||||||
| chr1:183328767
|
C | A | 1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.86-34974G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328767 | ||||||
| chr1:183328795
|
C | T | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35002G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328795 | ||||||
| chr1:183328796
|
A | G | 190 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.86-35003T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328796 | ||||||
| chr1:183328873
|
C | T | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35080G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328873 | ||||||
| chr1:183328914
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35121C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183328914 | ||||||
| chr1:183329015
|
G | A | 190 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.86-35222C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329015 | ||||||
| chr1:183329084
|
G | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35291C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329084 | ||||||
| chr1:183329207
|
C | T | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35414G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329207 | ||||||
| chr1:183329239
|
T | G | 22 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(19): Show | 22 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.86-35446A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329239 | ||||||
| chr1:183329256
|
G | A | 12 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0251others(9): Show | 12 | HG01123.hp2 HG01192.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-35463C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329256 | ||||||
| chr1:183329328
|
G | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35535C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329328 | ||||||
| chr1:183329344
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0039g0050 | 2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.86-35551A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329344 | ||||||
| chr1:183329360
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35567A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329360 | ||||||
| chr1:183329367
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35574A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329367 | ||||||
| chr1:183329475
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-35682A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329475 | ||||||
| chr1:183329610
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-35817G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329610 | ||||||
| chr1:183329683
|
T | G | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-35890A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329683 | ||||||
| chr1:183329717
|
A | C | 3 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.86-35924T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329717 | ||||||
| chr1:183329878
|
A | G | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-36085T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329878 | ||||||
| chr1:183329997
|
G | A | 1 | a0001c0001t0004g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.86-36204C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183329997 | ||||||
| chr1:183330018
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-36225C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330018 | ||||||
| chr1:183330367
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-36574C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330367 | ||||||
| chr1:183330382
|
G | T | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-36589C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330382 | ||||||
| chr1:183330476
|
A | G | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-36683T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330476 | ||||||
| chr1:183330488
|
T | C | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-36695A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330488 | ||||||
| chr1:183330489
|
G | A | 1 | a0001c0001t0024g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.86-36696C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330489 | ||||||
| chr1:183330492
|
C | G | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-36699G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330492 | ||||||
| chr1:183330512
|
C | A | 1 | a0001c0001t0002g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.86-36719G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330512 | ||||||
| chr1:183330666
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.86-36873T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330666 | ||||||
| chr1:183330737
|
T | G | 1 | a0001c0001t0007g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.86-36944A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330737 | ||||||
| chr1:183330746
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-36953A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330746 | ||||||
| chr1:183330839
|
A | G | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-37046T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330839 | ||||||
| chr1:183330915
|
T | A | 2 | a0001c0001t0004g0054a0001c0001t0005g0055 | 2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.86-37122A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330915 | ||||||
| chr1:183330977
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-37184A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183330977 | ||||||
| chr1:183331035
|
C | T | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-37242G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331035 | ||||||
| chr1:183331056
|
A | C | 1 | a0001c0001t0003g0065 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.86-37263T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331056 | ||||||
| chr1:183331135
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.86-37342T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331135 | ||||||
| chr1:183331176
|
A | G | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-37383T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331176 | ||||||
| chr1:183331241
|
A | AC | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-37449_86-37448i others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331241 | ||||||
| chr1:183331380
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.86-37587C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331380 | ||||||
| chr1:183331666
|
C | A | 1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.86-37873G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331666 | ||||||
| chr1:183331691
|
A | G | 20 | a0001c0001t0002g0082a0001c0001t0002g0199a0001c0001t0004g0233others(17): Show | 20 | HG01069.hp1 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.86-37898T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331691 | ||||||
| chr1:183331740
|
G | C | 2 | a0001c0001t0007g0019a0001c0001t0007g0020 | 2 | NA18950.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.86-37947C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331740 | ||||||
| chr1:183331759
|
G | C | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-37966C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183331759 | ||||||
| chr1:183332092
|
C | T | 1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.86-38299G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332092 | ||||||
| chr1:183332323
|
T | C | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-38530A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332323 | ||||||
| chr1:183332360
|
T | C | 5 | a0001c0001t0002g0037a0001c0001t0002g0164a0001c0001t0003g0187others(2): Show | 5 | HG00099.hp1 HG01516.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-38567A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332360 | ||||||
| chr1:183332407
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-38614C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332407 | ||||||
| chr1:183332822
|
C | A | 1 | a0001c0001t0031g0056 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.86-39029G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332822 | ||||||
| chr1:183332832
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-39039C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332832 | ||||||
| chr1:183332976
|
T | C | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-39183A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183332976 | ||||||
| chr1:183333074
|
C | A | 1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.86-39281G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333074 | ||||||
| chr1:183333147
|
T | C | 1 | a0001c0001t0078g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.86-39354A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333147 | ||||||
| chr1:183333237
|
G | C | 3 | a0001c0001t0005g0239a0001c0001t0009g0084a0001c0001t0017g0002 | 3 | HG02280.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.86-39444C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333237 | ||||||
| chr1:183333310
|
T | C | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-39517A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333310 | ||||||
| chr1:183333355
|
T | C | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-39562A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333355 | ||||||
| chr1:183333446
|
G | A | 1 | a0001c0001t0080g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.86-39653C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333446 | ||||||
| chr1:183333470
|
T | C | 97 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.86-39677A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333470 | ||||||
| chr1:183333653
|
G | GT | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-39861dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333653 | ||||||
| chr1:183333756
|
TAACTC | T | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-39968_86-39964d others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333756 | ||||||
| chr1:183333844
|
T | C | 89 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.86-40051A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183333844 | ||||||
| chr1:183334217
|
A | C | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40424T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334217 | ||||||
| chr1:183334291
|
T | C | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.86-40498A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334291 | ||||||
| chr1:183334308
|
C | A | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-40515G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334308 | ||||||
| chr1:183334332
|
G | T | 29 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(26): Show | 29 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.86-40539C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334332 | ||||||
| chr1:183334402
|
C | A | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40609G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334402 | ||||||
| chr1:183334424
|
C | T | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-40631G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334424 | ||||||
| chr1:183334467
|
C | T | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.86-40674G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334467 | ||||||
| chr1:183334508
|
C | T | 2 | a0001c0001t0016g0253a0001c0001t0028g0255 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.86-40715G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334508 | ||||||
| chr1:183334595
|
C | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40802G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334595 | ||||||
| chr1:183334641
|
T | C | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40848A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334641 | ||||||
| chr1:183334656
|
C | T | 6 | a0001c0001t0002g0082a0001c0001t0004g0233a0001c0001t0004g0236others(3): Show | 6 | HG01891.hp2 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-40863G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334656 | ||||||
| chr1:183334664
|
C | A | 3 | a0001c0001t0009g0078a0001c0001t0012g0080a0001c0001t0038g0079 | 3 | NA18975.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.86-40871G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334664 | ||||||
| chr1:183334693
|
G | A | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40900C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334693 | ||||||
| chr1:183334702
|
G | A | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-40909C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334702 | ||||||
| chr1:183334799
|
C | T | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(4): Show | 7 | HG00738.hp2 HG01952.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-41006G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334799 | ||||||
| chr1:183334806
|
G | A | 3 | a0001c0001t0014g0070a0001c0001t0014g0071a0001c0001t0014g0072 | 3 | NA18968.hp2 NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.86-41013C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334806 | ||||||
| chr1:183334881
|
C | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-41088G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183334881 | ||||||
| chr1:183335058
|
C | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-41265G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335058 | ||||||
| chr1:183335115
|
G | C | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-41322C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335115 | ||||||
| chr1:183335259
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-41466C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335259 | ||||||
| chr1:183335393
|
T | G | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-41600A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335393 | ||||||
| chr1:183335471
|
T | C | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.86-41678A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335471 | ||||||
| chr1:183335564
|
A | G | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-41771T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335564 | ||||||
| chr1:183335721
|
C | T | 2 | a0001c0001t0008g0121a0001c0001t0008g0122 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.86-41928G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183335721 | ||||||
| chr1:183336149
|
C | T | 9 | a0001c0001t0003g0030a0001c0001t0004g0054a0001c0001t0005g0055others(6): Show | 9 | HG00140.hp2 HG01258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-42356G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336149 | ||||||
| chr1:183336179
|
T | A | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.86-42386A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336179 | ||||||
| chr1:183336300
|
T | C | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-42507A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336300 | ||||||
| chr1:183336329
|
G | A | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-42536C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336329 | ||||||
| chr1:183336604
|
G | A | 5 | a0001c0001t0003g0046a0001c0001t0003g0065a0001c0001t0005g0047others(2): Show | 5 | HG00438.hp2 NA18946.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-42811C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336604 | ||||||
| chr1:183336889
|
C | T | 11 | a0001c0001t0002g0086a0001c0001t0002g0250a0001c0001t0004g0251others(8): Show | 11 | HG01123.hp2 HG01192.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-43096G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183336889 | ||||||
| chr1:183337276
|
AT | A | 4 | a0001c0001t0032g0108a0001c0001t0032g0184a0001c0001t0033g0110others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-43484delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337276 | ||||||
| chr1:183337279
|
A | G | 4 | a0001c0001t0032g0108a0001c0001t0032g0184a0001c0001t0033g0110others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-43486T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337279 | ||||||
| chr1:183337303
|
C | T | 9 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-43510G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337303 | ||||||
| chr1:183337330
|
G | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-43537C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337330 | ||||||
| chr1:183337350
|
C | A | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-43557G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337350 | ||||||
| chr1:183337389
|
C | T | 4 | a0001c0001t0003g0160a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG01106.hp1 HG01192.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-43596G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337389 | ||||||
| chr1:183337533
|
C | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-43740G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337533 | ||||||
| chr1:183337569
|
C | CA | 22 | a0001c0001t0001g0045a0001c0001t0001g0139a0001c0001t0002g0086others(19): Show | 22 | HG01123.hp2 HG01192.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.86-43777dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337569 | ||||||
| chr1:183337569
|
C | CAA | 18 | a0001c0001t0001g0242a0001c0001t0002g0149a0001c0001t0003g0032others(15): Show | 18 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-43778_86-43777d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337569 | ||||||
| chr1:183337569
|
C | CAAA | 101 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0227others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.86-43779_86-43777d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337569 | ||||||
| chr1:183337569
|
C | CAAAA | 14 | a0001c0001t0003g0064a0001c0001t0004g0178a0001c0001t0005g0047others(11): Show | 14 | HG00423.hp1 HG01081.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.86-43780_86-43777d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337569 | ||||||
| chr1:183337687
|
G | A | 1 | a0001c0001t0061g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.86-43894C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337687 | ||||||
| chr1:183337816
|
C | A | 1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.86-44023G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337816 | ||||||
| chr1:183337989
|
A | G | 1 | a0001c0001t0088g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.86-44196T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183337989 | ||||||
| chr1:183338012
|
T | C | 198 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(195): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.86-44219A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338012 | ||||||
| chr1:183338149
|
T | TA | 5 | a0001c0001t0001g0242a0001c0001t0011g0192a0001c0001t0017g0002others(2): Show | 5 | HG02055.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-44357dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAA | 27 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(24): Show | 27 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.86-44358_86-44357d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAAA | 32 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0199others(29): Show | 32 | HG01069.hp1 HG01123.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.86-44359_86-44357d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAAAA | 10 | a0001c0001t0002g0158a0001c0001t0007g0183a0001c0001t0011g0015others(7): Show | 10 | HG01070.hp2 HG01109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.86-44360_86-44357d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAAAAA | 23 | a0001c0001t0003g0029a0001c0001t0003g0156a0001c0001t0003g0160others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.86-44361_86-44357d others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAAAAAA | 97 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(94): Show | 97 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.86-44362_86-44357d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338149
|
T | TAAAAAAA | 5 | a0001c0001t0020g0095a0001c0001t0024g0099a0001c0001t0039g0050others(2): Show | 5 | HG00609.hp1 HG01978.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-44363_86-44357d others(9): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338149 | ||||||
| chr1:183338173
|
A | C | 1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.86-44380T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338173 | ||||||
| chr1:183338208
|
T | A | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44415A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338208 | ||||||
| chr1:183338218
|
C | CTATGATA others(13): Show |
195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44426_86-44425i others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338218 | ||||||
| chr1:183338221
|
T | A | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44428A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338221 | ||||||
| chr1:183338222
|
A | T | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44429T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338222 | ||||||
| chr1:183338223
|
A | G | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44430T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338223 | ||||||
| chr1:183338381
|
T | TG | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44589dupC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338381 | ||||||
| chr1:183338383
|
A | G | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44590T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338383 | ||||||
| chr1:183338413
|
T | C | 1 | a0001c0001t0024g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.86-44620A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338413 | ||||||
| chr1:183338535
|
A | G | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-44742T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338535 | ||||||
| chr1:183338553
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.86-44760A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338553 | ||||||
| chr1:183338595
|
T | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-44802A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338595 | ||||||
| chr1:183338724
|
G | T | 11 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0253others(8): Show | 11 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-44931C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338724 | ||||||
| chr1:183338739
|
A | C | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-44946T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338739 | ||||||
| chr1:183338807
|
A | G | 196 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(193): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.86-45014T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338807 | ||||||
| chr1:183338908
|
C | T | 1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.86-45115G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183338908 | ||||||
| chr1:183339015
|
A | C | 20 | a0001c0001t0005g0239a0001c0001t0009g0084a0001c0001t0009g0143others(17): Show | 20 | HG01109.hp2 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.86-45222T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339015 | ||||||
| chr1:183339166
|
C | T | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-45373G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339166 | ||||||
| chr1:183339336
|
A | T | 1 | a0001c0001t0012g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.86-45543T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339336 | ||||||
| chr1:183339344
|
G | A | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-45551C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339344 | ||||||
| chr1:183339378
|
A | T | 194 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(191): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.86-45585T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339378 | ||||||
| chr1:183339388
|
C | T | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.86-45595G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339388 | ||||||
| chr1:183339413
|
G | A | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-45620C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339413 | ||||||
| chr1:183339525
|
ACTGGGTT others(446): Show |
A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-46185_86-45733d others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339525 | ||||||
| chr1:183339652
|
A | G | 188 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.86-45859T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339652 | ||||||
| chr1:183339773
|
C | CA | 188 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.86-45981dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339773 | ||||||
| chr1:183339807
|
C | T | 185 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.86-46014G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339807 | ||||||
| chr1:183339888
|
C | A | 188 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.86-46095G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339888 | ||||||
| chr1:183339966
|
A | T | 188 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.86-46173T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339966 | ||||||
| chr1:183339979
|
C | G | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-46186G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339979 | ||||||
| chr1:183339980
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-46187C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183339980 | ||||||
| chr1:183340132
|
C | T | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.86-46339G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340132 | ||||||
| chr1:183340313
|
T | C | 1 | a0001c0001t0031g0056 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.86-46520A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340313 | ||||||
| chr1:183340321
|
CT | C | 182 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.86-46529delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340321 | ||||||
| chr1:183340321
|
CTT | C | 10 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.86-46530_86-46529d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340321 | ||||||
| chr1:183340331
|
T | C | 23 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.86-46538A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340331 | ||||||
| chr1:183340384
|
G | A | 192 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.86-46591C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340384 | ||||||
| chr1:183340566
|
C | T | 2 | a0001c0001t0002g0219a0001c0001t0009g0220 | 2 | HG03453.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.86-46773G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340566 | ||||||
| chr1:183340659
|
G | A | 2 | a0001c0001t0003g0163a0001c0001t0035g0161 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.86-46866C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340659 | ||||||
| chr1:183340683
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-46890A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183340683 | ||||||
| chr1:183341001
|
C | T | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-47208G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341001 | ||||||
| chr1:183341041
|
C | G | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-47248G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341041 | ||||||
| chr1:183341058
|
A | G | 8 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-47265T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341058 | ||||||
| chr1:183341165
|
C | T | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-47372G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341165 | ||||||
| chr1:183341191
|
G | A | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-47398C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341191 | ||||||
| chr1:183341199
|
C | A | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-47406G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341199 | ||||||
| chr1:183341523
|
C | CA | 9 | a0001c0001t0001g0228a0001c0001t0003g0217a0001c0001t0009g0143others(6): Show | 9 | HG01123.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-47731dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341523 | ||||||
| chr1:183341523
|
CA | C | 57 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0002g0158others(54): Show | 57 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.86-47731delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341523 | ||||||
| chr1:183341523
|
CAA | C | 122 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.86-47732_86-47731d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341523 | ||||||
| chr1:183341536
|
A | T | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-47743T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341536 | ||||||
| chr1:183341686
|
A | AG | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-47894_86-47893i others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341686 | ||||||
| chr1:183341686
|
AAG | A | 181 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.86-47895_86-47894d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341686 | ||||||
| chr1:183341687
|
AG | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-47895delC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341687 | ||||||
| chr1:183341687
|
AGAG | A | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-47897_86-47895d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341687 | ||||||
| chr1:183341690
|
G | A | 181 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(178): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.86-47897C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341690 | ||||||
| chr1:183341725
|
C | A | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-47932G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CA | 13 | a0001c0001t0002g0164a0001c0001t0004g0211a0001c0001t0006g0195others(10): Show | 13 | HG01516.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.86-47933dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAA | 17 | a0001c0001t0001g0136a0001c0001t0002g0158a0001c0001t0003g0156others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.86-47934_86-47933d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0035g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.86-47942_86-47933d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0010g0066a0001c0001t0079g0177 | 2 | HG03490.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-47944_86-47933d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0002g0250a0001c0001t0020g0247a0001c0001t0037g0252others(1): Show | 4 | HG02809.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-47945_86-47933d others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0086a0001c0001t0003g0064a0001c0001t0004g0251 | 3 | HG02717.hp1 HG02818.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.86-47946_86-47933d others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0073g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.86-47948_86-47933d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0007g0020a0001c0001t0007g0021a0001c0001t0007g0022 | 3 | NA18983.hp1 NA19012.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.86-47949_86-47933d others(19): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0007g0019a0001c0001t0007g0183a0001c0001t0014g0023 | 3 | NA18950.hp1 NA18956.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.86-47950_86-47933d others(20): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0046g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-47951_86-47933d others(21): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.86-47953_86-47933d others(23): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(15): Show |
17 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0139others(14): Show | 17 | HG00140.hp1 HG00423.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.86-47954_86-47933d others(24): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(16): Show |
28 | a0001c0001t0001g0045a0001c0001t0001g0128a0001c0001t0001g0140others(25): Show | 28 | HG00735.hp1 HG00738.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.86-47933_86-47932i others(25): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(17): Show |
21 | a0001c0001t0001g0035a0001c0001t0001g0130a0001c0001t0001g0132others(18): Show | 21 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.86-47933_86-47932i others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(18): Show |
18 | a0001c0001t0001g0101a0001c0001t0001g0227a0001c0001t0003g0032others(15): Show | 18 | HG00280.hp1 HG00609.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-47933_86-47932i others(27): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(19): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0137a0001c0001t0015g0040others(3): Show | 6 | HG00609.hp2 HG01978.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-47933_86-47932i others(28): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0001g0036 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.86-47933_86-47932i others(29): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.86-47933_86-47932i others(30): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(22): Show |
2 | a0001c0001t0010g0009a0001c0001t0054g0060 | 2 | HG01981.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.86-47933_86-47932i others(31): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0004g0054a0001c0001t0005g0055 | 2 | HG00140.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.86-47933_86-47932i others(34): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0013g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.86-47933_86-47932i others(35): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.86-47933_86-47932i others(34): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0016g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.86-47933_86-47932i others(31): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.86-47933_86-47932i others(32): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0006g0100a0001c0001t0013g0090 | 2 | NA18943.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.86-47933_86-47932i others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341725
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.86-47933_86-47932i others(27): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341725 | ||||||
| chr1:183341729
|
A | AAACAAAA others(7): Show |
1 | a0001c0001t0017g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.86-47937_86-47936i others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341729 | ||||||
| chr1:183341736
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-47944_86-47943i others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341736 | ||||||
| chr1:183341736
|
A | AAAACAAA others(9): Show |
3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-47944_86-47943i others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341736 | ||||||
| chr1:183341739
|
A | AAAACAAA others(7): Show |
4 | a0001c0001t0017g0173a0001c0001t0017g0176a0001c0001t0048g0174others(1): Show | 4 | HG02970.hp1 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-47947_86-47946i others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341739 | ||||||
| chr1:183341739
|
A | C | 1 | a0001c0001t0017g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.86-47946T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341739 | ||||||
| chr1:183341740
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0006 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.86-47948_86-47947i others(24): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341740 | ||||||
| chr1:183341742
|
A | AAAAAAAA others(10): Show |
6 | a0001c0001t0002g0199a0001c0001t0011g0015a0001c0001t0016g0256others(3): Show | 6 | HG01891.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-47950_86-47949i others(19): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341742 | ||||||
| chr1:183341742
|
A | AAAAAAAA others(9): Show |
3 | a0001c0001t0016g0253a0001c0001t0016g0254a0001c0001t0091g0257 | 3 | HG02109.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.86-47950_86-47949i others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341742 | ||||||
| chr1:183341742
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.86-47950_86-47949i others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341742 | ||||||
| chr1:183341742
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0028g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.86-47950_86-47949i others(13): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341742 | ||||||
| chr1:183341748
|
C | A | 185 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(182): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.86-47955G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341748 | ||||||
| chr1:183341748
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.86-47956_86-47955i others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341748 | ||||||
| chr1:183341846
|
A | G | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-48053T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341846 | ||||||
| chr1:183341946
|
C | T | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.86-48153G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183341946 | ||||||
| chr1:183342022
|
C | CT | 56 | a0001c0001t0002g0086a0001c0001t0002g0158a0001c0001t0002g0199others(53): Show | 56 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.86-48230dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342022 | ||||||
| chr1:183342022
|
CT | C | 128 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(125): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.86-48230delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342022 | ||||||
| chr1:183342022
|
CTTT | C | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-48232_86-48230d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342022 | ||||||
| chr1:183342024
|
T | A | 1 | a0001c0001t0004g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.86-48231A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342024 | ||||||
| chr1:183342125
|
C | A | 7 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0011g0103others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-48332G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342125 | ||||||
| chr1:183342630
|
C | T | 22 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0250others(19): Show | 22 | HG01123.hp2 HG01192.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.86-48837G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342630 | ||||||
| chr1:183342879
|
A | G | 1 | a0001c0001t0012g0215 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.86-49086T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342879 | ||||||
| chr1:183342899
|
A | AATT | 5 | a0001c0001t0002g0210a0001c0001t0002g0221a0001c0001t0002g0222others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-49109_86-49107d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342899 | ||||||
| chr1:183342899
|
AATT | A | 190 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(187): Show | 190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.86-49109_86-49107d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183342899 | ||||||
| chr1:183343129
|
C | G | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-49336G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343129 | ||||||
| chr1:183343198
|
C | T | 23 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.86-49405G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343198 | ||||||
| chr1:183343347
|
A | G | 1 | a0001c0001t0025g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.86-49554T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343347 | ||||||
| chr1:183343508
|
G | C | 1 | a0001c0001t0002g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.86-49715C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343508 | ||||||
| chr1:183343692
|
A | G | 9 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(6): Show | 9 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-49899T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343692 | ||||||
| chr1:183343747
|
A | G | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.86-49954T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343747 | ||||||
| chr1:183343804
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-50011G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183343804 | ||||||
| chr1:183344037
|
C | T | 1 | a0001c0001t0015g0040 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.86-50244G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344037 | ||||||
| chr1:183344103
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.86-50310C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344103 | ||||||
| chr1:183344210
|
G | A | 3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-50417C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344210 | ||||||
| chr1:183344232
|
C | A | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-50439G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344232 | ||||||
| chr1:183344260
|
C | T | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-50467G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344260 | ||||||
| chr1:183344262
|
T | C | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-50469A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344262 | ||||||
| chr1:183344687
|
G | T | 1 | a0001c0001t0007g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.86-50894C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344687 | ||||||
| chr1:183344705
|
T | C | 1 | a0001c0001t0007g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.86-50912A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344705 | ||||||
| chr1:183344753
|
C | T | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-50960G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344753 | ||||||
| chr1:183344777
|
T | C | 72 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.86-50984A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344777 | ||||||
| chr1:183344876
|
T | C | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-51083A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344876 | ||||||
| chr1:183344891
|
T | C | 195 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.86-51098A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344891 | ||||||
| chr1:183344897
|
C | T | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.86-51104G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183344897 | ||||||
| chr1:183345114
|
C | A | 3 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0076g0234 | 3 | HG02896.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-51321G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345114 | ||||||
| chr1:183345118
|
TCTC | T | 122 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.86-51328_86-51326d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345118 | ||||||
| chr1:183345158
|
G | T | 122 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.86-51365C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345158 | ||||||
| chr1:183345506
|
T | A | 130 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0101others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.86-51713A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345506 | ||||||
| chr1:183345688
|
CT | C | 204 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.86-51896delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345688 | ||||||
| chr1:183345773
|
G | A | 3 | a0001c0001t0032g0108a0001c0001t0032g0184a0001c0001t0089g0085 | 3 | HG01123.hp2 HG01192.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.86-51980C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345773 | ||||||
| chr1:183345987
|
A | T | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-52194T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183345987 | ||||||
| chr1:183346019
|
G | A | 1 | a0001c0001t0079g0177 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.86-52226C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346019 | ||||||
| chr1:183346096
|
C | G | 1 | a0001c0001t0075g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86-52303G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346096 | ||||||
| chr1:183346296
|
C | T | 5 | a0001c0001t0002g0082a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-52503G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346296 | ||||||
| chr1:183346348
|
A | G | 199 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.86-52555T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346348 | ||||||
| chr1:183346427
|
T | A | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.86-52634A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346427 | ||||||
| chr1:183346710
|
T | G | 4 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0017others(1): Show | 4 | HG01109.hp2 HG03041.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-52917A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183346710 | ||||||
| chr1:183347088
|
T | A | 12 | a0001c0001t0002g0153a0001c0001t0003g0029a0001c0001t0004g0178others(9): Show | 12 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-53295A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347088 | ||||||
| chr1:183347193
|
G | A | 71 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(68): Show | 71 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.86-53400C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347193 | ||||||
| chr1:183347255
|
A | G | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.86-53462T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347255 | ||||||
| chr1:183347324
|
T | C | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-53531A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347324 | ||||||
| chr1:183347376
|
A | G | 5 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(2): Show | 5 | HG02717.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-53583T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347376 | ||||||
| chr1:183347462
|
A | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-53669T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347462 | ||||||
| chr1:183347474
|
A | G | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-53681T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347474 | ||||||
| chr1:183347589
|
A | G | 7 | a0001c0001t0011g0015a0001c0001t0016g0175a0001c0001t0025g0014others(4): Show | 7 | HG01069.hp1 HG01109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-53796T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347589 | ||||||
| chr1:183347920
|
A | G | 1 | a0001c0001t0052g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.86-54127T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347920 | ||||||
| chr1:183347933
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.86-54140C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183347933 | ||||||
| chr1:183348274
|
G | A | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-54481C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183348274 | ||||||
| chr1:183348335
|
G | A | 22 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(19): Show | 22 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.86-54542C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183348335 | ||||||
| chr1:183348586
|
A | T | 1 | a0001c0001t0002g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.86-54793T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183348586 | ||||||
| chr1:183348684
|
T | G | 95 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.86-54891A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183348684 | ||||||
| chr1:183349469
|
C | T | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.86-55676G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183349469 | ||||||
| chr1:183349565
|
C | T | 12 | a0001c0001t0002g0153a0001c0001t0003g0029a0001c0001t0004g0178others(9): Show | 12 | HG01106.hp2 HG01257.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-55772G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183349565 | ||||||
| chr1:183349654
|
G | A | 1 | a0001c0001t0004g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.86-55861C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183349654 | ||||||
| chr1:183349934
|
C | G | 6 | a0001c0001t0002g0199a0001c0001t0016g0253a0001c0001t0016g0254others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-56141G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183349934 | ||||||
| chr1:183350095
|
G | A | 1 | a0001c0001t0012g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-56302C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350095 | ||||||
| chr1:183350138
|
G | C | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-56345C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350138 | ||||||
| chr1:183350170
|
G | A | 1 | a0001c0001t0075g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.86-56377C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350170 | ||||||
| chr1:183350390
|
G | A | 1 | a0001c0001t0040g0205 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.86-56597C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350390 | ||||||
| chr1:183350545
|
C | A | 2 | a0001c0001t0002g0049a0001c0001t0039g0050 | 2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.86-56752G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350545 | ||||||
| chr1:183350867
|
A | G | 1 | a0001c0001t0007g0022 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.86-57074T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350867 | ||||||
| chr1:183350899
|
G | C | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.86-57106C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350899 | ||||||
| chr1:183350908
|
C | G | 1 | a0001c0001t0012g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.86-57115G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350908 | ||||||
| chr1:183350911
|
T | A | 3 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0037g0252 | 3 | HG02717.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.86-57118A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350911 | ||||||
| chr1:183350964
|
C | G | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-57171G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183350964 | ||||||
| chr1:183351040
|
G | A | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.86-57247C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351040 | ||||||
| chr1:183351044
|
T | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-57251A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351044 | ||||||
| chr1:183351057
|
C | T | 140 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.86-57264G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351057 | ||||||
| chr1:183351256
|
A | C | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.86-57463T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351256 | ||||||
| chr1:183351343
|
T | C | 8 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0009g0084others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-57550A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351343 | ||||||
| chr1:183351558
|
A | G | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.86-57765T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351558 | ||||||
| chr1:183351711
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-57918C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351711 | ||||||
| chr1:183351901
|
G | C | 1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.86-58108C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183351901 | ||||||
| chr1:183352040
|
T | C | 2 | a0001c0001t0009g0078a0001c0001t0012g0080 | 2 | NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.86-58247A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352040 | ||||||
| chr1:183352133
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-58340C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352133 | ||||||
| chr1:183352435
|
C | T | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.86-58642G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352435 | ||||||
| chr1:183352494
|
C | T | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-58701G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352494 | ||||||
| chr1:183352562
|
C | CA | 8 | a0001c0001t0004g0006a0001c0001t0006g0195a0001c0001t0011g0192others(5): Show | 8 | HG01109.hp2 HG01978.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.86-58770dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352562 | ||||||
| chr1:183352562
|
CA | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.86-58770delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352562 | ||||||
| chr1:183352562
|
CAA | C | 9 | a0001c0001t0002g0158a0001c0001t0003g0032a0001c0001t0011g0015others(6): Show | 9 | HG01069.hp1 HG01070.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-58771_86-58770d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352562 | ||||||
| chr1:183352562
|
CAAAAAAA others(1): Show |
C | 36 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(33): Show | 36 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.86-58777_86-58770d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352562 | ||||||
| chr1:183352742
|
C | T | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.86-58949G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352742 | ||||||
| chr1:183352956
|
G | A | 1 | a0001c0001t0013g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.86-59163C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352956 | ||||||
| chr1:183352957
|
G | A | 1 | a0001c0001t0013g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.86-59164C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183352957 | ||||||
| chr1:183353089
|
C | T | 2 | a0001c0001t0003g0163a0001c0001t0035g0161 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.86-59296G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353089 | ||||||
| chr1:183353182
|
A | G | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.86-59389T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353182 | ||||||
| chr1:183353283
|
G | A | 1 | a0001c0001t0051g0081 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.86-59490C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353283 | ||||||
| chr1:183353641
|
C | T | 1 | a0001c0001t0013g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.86-59848G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353641 | ||||||
| chr1:183353843
|
T | C | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.86-60050A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353843 | ||||||
| chr1:183353866
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.86-60073A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353866 | ||||||
| chr1:183353888
|
T | C | 7 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0011g0103others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-60095A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183353888 | ||||||
| chr1:183354354
|
G | A | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.86-60561C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354354 | ||||||
| chr1:183354409
|
C | CT | 9 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0006g0229others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-60617dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354409 | ||||||
| chr1:183354409
|
CT | C | 36 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(33): Show | 36 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.86-60617delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354409 | ||||||
| chr1:183354409
|
CTT | C | 124 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.86-60618_86-60617d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354409 | ||||||
| chr1:183354409
|
CTTT | C | 12 | a0001c0001t0003g0032a0001c0001t0003g0046a0001c0001t0003g0062others(9): Show | 12 | HG00438.hp2 HG01069.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-60619_86-60617d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354409 | ||||||
| chr1:183354499
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-60706G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354499 | ||||||
| chr1:183354508
|
C | T | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(70): Show | 73 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.86-60715G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354508 | ||||||
| chr1:183354573
|
A | G | 140 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.86-60780T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354573 | ||||||
| chr1:183354582
|
T | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.86-60789A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354582 | ||||||
| chr1:183354620
|
T | C | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.86-60827A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354620 | ||||||
| chr1:183354669
|
G | A | 73 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(70): Show | 73 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.86-60876C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183354669 | ||||||
| chr1:183355206
|
C | T | 1 | a0001c0001t0046g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.86-61413G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183355206 | ||||||
| chr1:183355219
|
T | C | 147 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.86-61426A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183355219 | ||||||
| chr1:183355268
|
GCCTCTTA others(6): Show |
G | 1 | a0001c0001t0037g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.86-61488_86-61476d others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183355268 | ||||||
| chr1:183355614
|
A | G | 6 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0142others(3): Show | 6 | HG02129.hp2 NA18947.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-61821T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183355614 | ||||||
| chr1:183356014
|
C | T | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.85+62169G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356014 | ||||||
| chr1:183356098
|
T | G | 7 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(4): Show | 7 | HG02451.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+62085A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356098 | ||||||
| chr1:183356117
|
G | A | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.85+62066C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356117 | ||||||
| chr1:183356281
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.85+61902G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356281 | ||||||
| chr1:183356315
|
A | G | 1 | a0001c0001t0038g0190 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.85+61868T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356315 | ||||||
| chr1:183356452
|
C | T | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.85+61731G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356452 | ||||||
| chr1:183356587
|
C | T | 147 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.85+61596G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356587 | ||||||
| chr1:183356643
|
T | C | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+61540A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356643 | ||||||
| chr1:183356661
|
T | G | 140 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.85+61522A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356661 | ||||||
| chr1:183356904
|
T | G | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+61279A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356904 | ||||||
| chr1:183356946
|
G | T | 6 | a0001c0001t0002g0199a0001c0001t0016g0253a0001c0001t0016g0254others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+61237C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183356946 | ||||||
| chr1:183357044
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.85+61139T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357044 | ||||||
| chr1:183357103
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.85+61080C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357103 | ||||||
| chr1:183357123
|
G | C | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+61060C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357123 | ||||||
| chr1:183357219
|
C | CT | 23 | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0242others(20): Show | 23 | HG00438.hp2 HG00735.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.85+60963dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357219 | ||||||
| chr1:183357219
|
CT | C | 68 | a0001c0001t0001g0045a0001c0001t0001g0124a0001c0001t0001g0125others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.85+60963delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357219 | ||||||
| chr1:183357268
|
C | T | 7 | a0001c0001t0011g0015a0001c0001t0016g0175a0001c0001t0025g0014others(4): Show | 7 | HG01069.hp1 HG01109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+60915G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357268 | ||||||
| chr1:183357353
|
C | G | 23 | a0001c0001t0001g0101a0001c0001t0004g0006a0001c0001t0004g0178others(20): Show | 23 | HG00423.hp2 HG01081.hp2 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.85+60830G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357353 | ||||||
| chr1:183357374
|
C | T | 1 | a0001c0001t0013g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+60809G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357374 | ||||||
| chr1:183357632
|
C | T | 1 | a0001c0001t0009g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+60551G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357632 | ||||||
| chr1:183357633
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.85+60550C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357633 | ||||||
| chr1:183357665
|
G | A | 1 | a0001c0001t0079g0177 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.85+60518C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357665 | ||||||
| chr1:183357693
|
A | G | 147 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.85+60490T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357693 | ||||||
| chr1:183357701
|
C | G | 11 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.85+60482G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357701 | ||||||
| chr1:183357701
|
C | T | 7 | a0001c0001t0011g0015a0001c0001t0016g0175a0001c0001t0025g0014others(4): Show | 7 | HG01069.hp1 HG01109.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+60482G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357701 | ||||||
| chr1:183357702
|
G | A | 1 | a0001c0001t0018g0197 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.85+60481C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357702 | ||||||
| chr1:183357791
|
G | A | 1 | a0001c0001t0024g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.85+60392C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357791 | ||||||
| chr1:183357961
|
C | T | 5 | a0001c0001t0004g0233a0001c0001t0004g0236a0001c0001t0027g0235others(2): Show | 5 | HG02886.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+60222G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183357961 | ||||||
| chr1:183358116
|
C | T | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+60067G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358116 | ||||||
| chr1:183358246
|
C | T | 1 | a0001c0001t0042g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85+59937G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358246 | ||||||
| chr1:183358293
|
A | G | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+59890T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358293 | ||||||
| chr1:183358424
|
T | C | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.85+59759A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358424 | ||||||
| chr1:183358731
|
C | T | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.85+59452G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358731 | ||||||
| chr1:183358836
|
C | T | 24 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(21): Show | 24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.85+59347G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183358836 | ||||||
| chr1:183359133
|
G | T | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85+59050C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183359133 | ||||||
| chr1:183359688
|
T | C | 2 | a0001c0001t0022g0240a0001c0001t0028g0218 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.85+58495A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183359688 | ||||||
| chr1:183359914
|
C | T | 1 | a0001c0001t0032g0108 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.85+58269G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183359914 | ||||||
| chr1:183360126
|
C | T | 5 | a0001c0001t0004g0054a0001c0001t0005g0055a0001c0001t0012g0039others(2): Show | 5 | HG00140.hp2 HG03942.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+58057G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360126 | ||||||
| chr1:183360345
|
C | A | 1 | a0001c0001t0004g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85+57838G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360345 | ||||||
| chr1:183360517
|
G | T | 1 | a0001c0001t0016g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.85+57666C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360517 | ||||||
| chr1:183360588
|
C | G | 1 | a0001c0001t0090g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.85+57595G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360588 | ||||||
| chr1:183360692
|
G | A | 4 | a0001c0001t0002g0219a0001c0001t0016g0175a0001c0001t0026g0004others(1): Show | 4 | HG01109.hp2 HG03041.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+57491C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360692 | ||||||
| chr1:183360900
|
A | G | 7 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(4): Show | 7 | HG02451.hp1 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+57283T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183360900 | ||||||
| chr1:183361120
|
T | C | 189 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.85+57063A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183361120 | ||||||
| chr1:183361278
|
G | T | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.85+56905C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183361278 | ||||||
| chr1:183361602
|
TAA | T | 140 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(137): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.85+56579_85+56580d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183361602 | ||||||
| chr1:183361621
|
C | G | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85+56562G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183361621 | ||||||
| chr1:183362016
|
C | A | 1 | a0001c0001t0035g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.85+56167G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362016 | ||||||
| chr1:183362088
|
G | T | 1 | a0001c0001t0007g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.85+56095C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362088 | ||||||
| chr1:183362372
|
C | T | 1 | a0001c0001t0022g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.85+55811G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362372 | ||||||
| chr1:183362394
|
A | C | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+55789T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362394 | ||||||
| chr1:183362554
|
G | A | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+55629C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362554 | ||||||
| chr1:183362725
|
C | T | 29 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0003g0160others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.85+55458G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362725 | ||||||
| chr1:183362865
|
A | G | 1 | a0001c0001t0013g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+55318T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362865 | ||||||
| chr1:183362883
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+55300G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183362883 | ||||||
| chr1:183363399
|
T | C | 1 | a0001c0001t0004g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.85+54784A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363399 | ||||||
| chr1:183363579
|
T | TAC | 122 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.85+54602_85+54603d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363579 | ||||||
| chr1:183363579
|
T | TACAC | 30 | a0001c0001t0003g0160a0001c0001t0003g0165a0001c0001t0003g0166others(27): Show | 30 | HG01069.hp1 HG01106.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.85+54600_85+54603d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363579 | ||||||
| chr1:183363579
|
T | TACACAC | 4 | a0001c0001t0011g0103a0001c0001t0016g0175a0001c0001t0026g0004others(1): Show | 4 | HG01109.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+54598_85+54603d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363579 | ||||||
| chr1:183363579
|
T | TACACACA others(1): Show |
7 | a0001c0001t0002g0158a0001c0001t0003g0156a0001c0001t0004g0152others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+54596_85+54603d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363579 | ||||||
| chr1:183363579
|
TAC | T | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(6): Show | 9 | HG02155.hp2 HG03831.hp2 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+54602_85+54603d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363579 | ||||||
| chr1:183363788
|
G | A | 1 | a0001c0002t0041g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.85+54395C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363788 | ||||||
| chr1:183363868
|
A | T | 6 | a0001c0001t0002g0199a0001c0001t0016g0253a0001c0001t0016g0254others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+54315T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183363868 | ||||||
| chr1:183364024
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.85+54159A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364024 | ||||||
| chr1:183364187
|
A | G | 1 | a0001c0001t0003g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.85+53996T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364187 | ||||||
| chr1:183364322
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.85+53861G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364322 | ||||||
| chr1:183364369
|
C | T | 1 | a0001c0001t0037g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+53814G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364369 | ||||||
| chr1:183364419
|
C | G | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.85+53764G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364419 | ||||||
| chr1:183364612
|
A | G | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+53571T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364612 | ||||||
| chr1:183364650
|
G | A | 88 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.85+53533C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364650 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(1): Show |
4 | a0001c0001t0003g0160a0001c0001t0003g0165a0001c0001t0003g0166others(1): Show | 4 | HG01106.hp1 HG01192.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+53520_85+53527d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(5): Show |
1 | a0001c0001t0059g0162 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.85+53516_85+53527d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(9): Show |
9 | a0001c0001t0003g0156a0001c0001t0004g0154a0001c0001t0011g0015others(6): Show | 9 | HG00099.hp2 HG01069.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(13): Show |
16 | a0001c0001t0002g0158a0001c0001t0003g0062a0001c0001t0004g0152others(13): Show | 16 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(17): Show |
19 | a0001c0001t0001g0036a0001c0001t0003g0032a0001c0001t0003g0064others(16): Show | 19 | HG00735.hp2 HG01109.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(21): Show |
27 | a0001c0001t0002g0013a0001c0001t0002g0199a0001c0001t0003g0029others(24): Show | 27 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(30): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(25): Show |
19 | a0001c0001t0001g0045a0001c0001t0002g0041a0001c0001t0002g0153others(16): Show | 19 | HG01106.hp2 HG01123.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(34): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(29): Show |
19 | a0001c0001t0001g0035a0001c0001t0003g0030a0001c0001t0004g0044others(16): Show | 19 | HG01169.hp1 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(38): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(33): Show |
4 | a0001c0001t0002g0086a0001c0001t0004g0054a0001c0001t0012g0039others(1): Show | 4 | HG00140.hp2 HG02109.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+53527_85+53528i others(42): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364655
|
A | ATTTCTTT others(41): Show |
1 | a0001c0001t0028g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.85+53527_85+53528i others(50): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364655 | ||||||
| chr1:183364670
|
A | T | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.85+53513T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364670 | ||||||
| chr1:183364680
|
T | TTTCTTTC others(28): Show |
1 | a0001c0001t0047g0075 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.85+53502_85+53503i others(37): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364680 | ||||||
| chr1:183364684
|
T | TTTCTTTC others(32): Show |
1 | a0001c0001t0002g0049 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.85+53498_85+53499i others(41): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364684 | ||||||
| chr1:183364685
|
T | TTCTTTCT others(35): Show |
1 | a0001c0001t0037g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+53497_85+53498i others(44): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364685 | ||||||
| chr1:183364686
|
T | TCTTTCTT others(26): Show |
2 | a0001c0001t0075g0063a0001c0001t0080g0053 | 2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.85+53496_85+53497i others(35): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364686 | ||||||
| chr1:183364972
|
C | A | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.85+53211G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183364972 | ||||||
| chr1:183365005
|
A | G | 3 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.85+53178T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365005 | ||||||
| chr1:183365015
|
A | G | 59 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(56): Show | 59 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.85+53168T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365015 | ||||||
| chr1:183365102
|
A | G | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85+53081T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365102 | ||||||
| chr1:183365243
|
A | T | 1 | a0001c0001t0013g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.85+52940T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365243 | ||||||
| chr1:183365303
|
G | T | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.85+52880C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365303 | ||||||
| chr1:183365795
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.85+52388G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365795 | ||||||
| chr1:183365845
|
G | A | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.85+52338C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365845 | ||||||
| chr1:183365900
|
A | C | 4 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(1): Show | 4 | HG02109.hp2 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+52283T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365900 | ||||||
| chr1:183365985
|
A | G | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.85+52198T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183365985 | ||||||
| chr1:183366188
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+51995G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366188 | ||||||
| chr1:183366255
|
C | T | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+51928G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366255 | ||||||
| chr1:183366332
|
T | C | 124 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.85+51851A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366332 | ||||||
| chr1:183366360
|
C | T | 117 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(114): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.85+51823G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366360 | ||||||
| chr1:183366582
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85+51601C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366582 | ||||||
| chr1:183366826
|
C | G | 1 | a0001c0001t0031g0131 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.85+51357G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366826 | ||||||
| chr1:183366910
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.85+51273G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183366910 | ||||||
| chr1:183367412
|
C | T | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.85+50771G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183367412 | ||||||
| chr1:183367442
|
G | A | 1 | a0001c0001t0031g0056 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.85+50741C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183367442 | ||||||
| chr1:183368115
|
T | A | 1 | a0001c0001t0041g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.85+50068A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368115 | ||||||
| chr1:183368257
|
C | T | 1 | a0001c0001t0094g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.85+49926G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368257 | ||||||
| chr1:183368318
|
G | A | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85+49865C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368318 | ||||||
| chr1:183368613
|
C | T | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+49570G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368613 | ||||||
| chr1:183368748
|
T | C | 5 | a0001c0001t0002g0037a0001c0001t0002g0164a0001c0001t0003g0187others(2): Show | 5 | HG00099.hp1 HG01516.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+49435A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368748 | ||||||
| chr1:183368798
|
A | G | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.85+49385T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368798 | ||||||
| chr1:183368916
|
C | T | 1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85+49267G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183368916 | ||||||
| chr1:183369072
|
G | T | 87 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(84): Show | 87 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.85+49111C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369072 | ||||||
| chr1:183369211
|
C | T | 3 | a0001c0001t0016g0175a0001c0001t0026g0004a0001c0001t0030g0169 | 3 | HG01109.hp2 HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85+48972G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369211 | ||||||
| chr1:183369237
|
T | C | 11 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.85+48946A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369237 | ||||||
| chr1:183369263
|
CT | C | 70 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(67): Show | 70 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.85+48919delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369263 | ||||||
| chr1:183369263
|
CTT | C | 33 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0003g0156others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.85+48918_85+48919d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369263 | ||||||
| chr1:183369263
|
CTTT | C | 86 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(83): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.85+48917_85+48919d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369263 | ||||||
| chr1:183369629
|
T | C | 1 | a0001c0001t0004g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.85+48554A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369629 | ||||||
| chr1:183369650
|
T | C | 3 | a0001c0001t0009g0220a0001c0001t0016g0194a0001c0001t0027g0185 | 3 | HG02145.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.85+48533A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369650 | ||||||
| chr1:183369691
|
G | A | 123 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.85+48492C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369691 | ||||||
| chr1:183369807
|
G | A | 2 | a0001c0001t0024g0087a0001c0001t0024g0099 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.85+48376C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369807 | ||||||
| chr1:183369939
|
C | T | 3 | a0001c0001t0006g0097a0001c0001t0006g0100a0001c0001t0013g0090 | 3 | NA18943.hp2 NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.85+48244G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183369939 | ||||||
| chr1:183370022
|
G | A | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+48161C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370022 | ||||||
| chr1:183370123
|
C | T | 1 | a0001c0001t0009g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.85+48060G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370123 | ||||||
| chr1:183370144
|
G | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+48039C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370144 | ||||||
| chr1:183370145
|
G | T | 15 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0009g0084others(12): Show | 15 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+48038C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370145 | ||||||
| chr1:183370223
|
T | TAC | 29 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0228others(26): Show | 29 | HG01123.hp1 HG01952.hp1 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.85+47958_85+47959d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TACAC | 24 | a0001c0001t0002g0041a0001c0001t0003g0156a0001c0001t0003g0160others(21): Show | 24 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.85+47956_85+47959d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TACACAC | 14 | a0001c0001t0002g0149a0001c0001t0002g0158a0001c0001t0003g0030others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.85+47954_85+47959d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TACACACA others(1): Show |
3 | a0001c0001t0009g0144a0001c0001t0023g0147a0001c0001t0026g0117 | 3 | HG02647.hp2 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85+47952_85+47959d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TACACACA others(3): Show |
4 | a0001c0001t0002g0049a0001c0001t0021g0145a0001c0001t0023g0148others(1): Show | 4 | HG01070.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+47950_85+47959d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TGCAC | 3 | a0001c0001t0010g0011a0001c0001t0014g0073a0001c0001t0072g0010 | 3 | HG01952.hp2 HG02148.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.85+47959_85+47960i others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
T | TGCACACA others(3): Show |
1 | a0001c0001t0002g0013 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.85+47959_85+47960i others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TAC | T | 53 | a0001c0001t0001g0036a0001c0001t0001g0136a0001c0001t0001g0242others(50): Show | 54 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.85+47958_85+47959d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACAC | T | 39 | a0001c0001t0002g0153a0001c0001t0002g0164a0001c0001t0002g0221others(36): Show | 39 | HG00099.hp1 HG01081.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.85+47956_85+47959d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACACAC | T | 5 | a0001c0001t0001g0045a0001c0001t0022g0024a0001c0001t0055g0188others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+47954_85+47959d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACACACA others(1): Show |
T | 10 | a0001c0001t0004g0154a0001c0001t0004g0178a0001c0001t0005g0104others(7): Show | 10 | HG01123.hp2 HG01192.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+47952_85+47959d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0029g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.85+47950_85+47959d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.85+47948_85+47959d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370223
|
TACACACA others(17): Show |
T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+47936_85+47959d others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370223 | ||||||
| chr1:183370594
|
G | A | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+47589C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370594 | ||||||
| chr1:183370712
|
A | G | 17 | a0001c0001t0002g0158a0001c0001t0002g0164a0001c0001t0003g0156others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.85+47471T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370712 | ||||||
| chr1:183370782
|
C | G | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+47401G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370782 | ||||||
| chr1:183370850
|
T | C | 192 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.85+47333A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370850 | ||||||
| chr1:183370994
|
G | C | 199 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(196): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.85+47189C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183370994 | ||||||
| chr1:183371094
|
A | T | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85+47089T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371094 | ||||||
| chr1:183371103
|
A | G | 118 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.85+47080T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371103 | ||||||
| chr1:183371227
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.85+46956T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371227 | ||||||
| chr1:183371303
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0028g0218 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.85+46880G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371303 | ||||||
| chr1:183371499
|
C | T | 10 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+46684G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371499 | ||||||
| chr1:183371542
|
C | T | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+46641G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371542 | ||||||
| chr1:183371770
|
G | A | 8 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0009g0084others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+46413C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183371770 | ||||||
| chr1:183372233
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+45950G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372233 | ||||||
| chr1:183372345
|
A | C | 1 | a0001c0001t0003g0213 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.85+45838T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372345 | ||||||
| chr1:183372745
|
C | T | 1 | a0001c0001t0005g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.85+45438G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372745 | ||||||
| chr1:183372769
|
C | T | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.85+45414G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372769 | ||||||
| chr1:183372922
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+45261G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372922 | ||||||
| chr1:183372950
|
C | T | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+45233G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372950 | ||||||
| chr1:183372999
|
C | A | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+45184G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183372999 | ||||||
| chr1:183373005
|
G | A | 3 | a0001c0001t0062g0225a0001c0001t0081g0200a0001c0001t0086g0206 | 3 | HG03239.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.85+45178C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373005 | ||||||
| chr1:183373277
|
C | T | 6 | a0001c0001t0002g0199a0001c0001t0016g0253a0001c0001t0016g0254others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+44906G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373277 | ||||||
| chr1:183373515
|
C | T | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+44668G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373515 | ||||||
| chr1:183373575
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+44608A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373575 | ||||||
| chr1:183373619
|
CT | C | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(61): Show | 64 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.85+44563delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373619 | ||||||
| chr1:183373708
|
C | T | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.85+44475G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373708 | ||||||
| chr1:183373719
|
G | C | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+44464C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373719 | ||||||
| chr1:183373722
|
A | C | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+44461T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373722 | ||||||
| chr1:183373758
|
C | T | 1 | a0001c0001t0069g0008 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.85+44425G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183373758 | ||||||
| chr1:183374099
|
T | G | 4 | a0001c0001t0005g0239a0001c0001t0017g0002a0001c0001t0090g0226others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+44084A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374099 | ||||||
| chr1:183374137
|
T | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+44046A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374137 | ||||||
| chr1:183374227
|
A | G | 98 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.85+43956T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374227 | ||||||
| chr1:183374266
|
A | C | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+43917T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374266 | ||||||
| chr1:183374296
|
A | AC | 92 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.85+43886dupG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374296 | ||||||
| chr1:183374379
|
T | C | 1 | a0001c0001t0010g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.85+43804A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374379 | ||||||
| chr1:183374391
|
A | T | 2 | a0001c0001t0020g0095a0001c0001t0020g0096 | 2 | NA18946.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.85+43792T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374391 | ||||||
| chr1:183374648
|
T | G | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+43535A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183374648 | ||||||
| chr1:183375085
|
A | C | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+43098T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375085 | ||||||
| chr1:183375124
|
C | A | 1 | a0001c0001t0009g0232 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.85+43059G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375124 | ||||||
| chr1:183375190
|
T | A | 1 | a0001c0001t0007g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.85+42993A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375190 | ||||||
| chr1:183375256
|
A | G | 2 | a0001c0001t0022g0240a0001c0001t0028g0218 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.85+42927T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375256 | ||||||
| chr1:183375570
|
G | A | 1 | a0001c0001t0003g0030 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.85+42613C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375570 | ||||||
| chr1:183375609
|
G | A | 1 | a0001c0001t0003g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.85+42574C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375609 | ||||||
| chr1:183375679
|
C | A | 4 | a0001c0001t0002g0086a0001c0001t0032g0108a0001c0001t0032g0184others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+42504G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375679 | ||||||
| chr1:183375798
|
T | TA | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+42384dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375798 | ||||||
| chr1:183375807
|
A | T | 1 | a0001c0001t0014g0073 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.85+42376T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183375807 | ||||||
| chr1:183376007
|
T | TA | 182 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.85+42175dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376007 | ||||||
| chr1:183376026
|
G | T | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.85+42157C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376026 | ||||||
| chr1:183376068
|
A | G | 91 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.85+42115T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376068 | ||||||
| chr1:183376212
|
T | C | 1 | a0001c0001t0009g0143 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.85+41971A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376212 | ||||||
| chr1:183376215
|
T | G | 91 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(88): Show | 91 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.85+41968A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376215 | ||||||
| chr1:183376238
|
G | A | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85+41945C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376238 | ||||||
| chr1:183376317
|
T | G | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.85+41866A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376317 | ||||||
| chr1:183376572
|
A | T | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+41611T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376572 | ||||||
| chr1:183376585
|
G | A | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+41598C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376585 | ||||||
| chr1:183376665
|
A | T | 5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+41518T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183376665 | ||||||
| chr1:183377023
|
C | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+41160G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377023 | ||||||
| chr1:183377062
|
T | C | 1 | a0001c0001t0018g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85+41121A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377062 | ||||||
| chr1:183377078
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+41105G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377078 | ||||||
| chr1:183377198
|
T | A | 1 | a0001c0001t0013g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+40985A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377198 | ||||||
| chr1:183377237
|
C | T | 1 | a0001c0001t0040g0205 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.85+40946G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377237 | ||||||
| chr1:183377336
|
A | T | 1 | a0001c0001t0005g0239 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85+40847T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377336 | ||||||
| chr1:183377534
|
T | C | 92 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.85+40649A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377534 | ||||||
| chr1:183377715
|
A | T | 4 | a0001c0001t0002g0199a0001c0001t0044g0196a0001c0001t0057g0249others(1): Show | 4 | HG01099.hp1 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+40468T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377715 | ||||||
| chr1:183377794
|
T | G | 4 | a0001c0001t0014g0070a0001c0001t0014g0071a0001c0001t0014g0072others(1): Show | 4 | NA18968.hp2 NA18983.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+40389A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377794 | ||||||
| chr1:183377999
|
C | A | 1 | a0001c0001t0034g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.85+40184G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183377999 | ||||||
| chr1:183378119
|
C | T | 78 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(75): Show | 78 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.85+40064G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378119 | ||||||
| chr1:183378189
|
T | C | 92 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.85+39994A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378189 | ||||||
| chr1:183378308
|
C | T | 2 | a0001c0001t0009g0084a0001c0001t0056g0151 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.85+39875G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378308 | ||||||
| chr1:183378381
|
G | A | 1 | a0001c0001t0024g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.85+39802C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378381 | ||||||
| chr1:183378385
|
C | T | 2 | a0001c0001t0022g0240a0001c0001t0028g0218 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.85+39798G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378385 | ||||||
| chr1:183378391
|
TA | T | 8 | a0001c0001t0005g0239a0001c0001t0011g0015a0001c0001t0016g0254others(5): Show | 8 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+39791delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378391 | ||||||
| chr1:183378429
|
C | T | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.85+39754G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378429 | ||||||
| chr1:183378703
|
A | G | 2 | a0001c0001t0008g0133a0001c0001t0008g0135 | 2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.85+39480T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378703 | ||||||
| chr1:183378742
|
C | T | 1 | a0001c0001t0053g0180 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.85+39441G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378742 | ||||||
| chr1:183378778
|
T | C | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+39405A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378778 | ||||||
| chr1:183378815
|
A | AG | 256 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(253): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.85+39367dupC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183378815 | ||||||
| chr1:183379047
|
A | AATATCT | 40 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0242others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.85+39130_85+39135d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379047 | ||||||
| chr1:183379047
|
A | AATATCTA others(5): Show |
6 | a0001c0001t0003g0212a0001c0001t0004g0216a0001c0001t0017g0173others(3): Show | 6 | HG01123.hp1 HG01167.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+39124_85+39135d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379047 | ||||||
| chr1:183379047
|
A | AATATCTA others(11): Show |
5 | a0001c0001t0006g0195a0001c0001t0017g0171a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+39118_85+39135d others(20): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379047 | ||||||
| chr1:183379047
|
AATATCT | A | 7 | a0001c0001t0002g0082a0001c0001t0011g0192a0001c0001t0033g0246others(4): Show | 7 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+39130_85+39135d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379047 | ||||||
| chr1:183379079
|
TATCTATA others(6): Show |
T | 2 | a0001c0001t0002g0086a0001c0001t0026g0004 | 2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85+39091_85+39103d others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379079 | ||||||
| chr1:183379085
|
TATCTATA | T | 40 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(37): Show | 40 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.85+39091_85+39097d others(9): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379085 | ||||||
| chr1:183379090
|
A | G | 1 | a0001c0001t0057g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.85+39093T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379090 | ||||||
| chr1:183379091
|
TA | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0128others(67): Show | 70 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.85+39091delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379091 | ||||||
| chr1:183379092
|
A | ATCTAT | 44 | a0001c0001t0001g0045a0001c0001t0002g0013a0001c0001t0002g0153others(41): Show | 44 | HG00280.hp2 HG00438.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.85+39090_85+39091i others(7): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379092 | ||||||
| chr1:183379092
|
A | ATCTATAT others(4): Show |
21 | a0001c0001t0002g0041a0001c0001t0002g0049a0001c0001t0003g0030others(18): Show | 21 | HG01070.hp1 HG01258.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.85+39090_85+39091i others(13): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379092 | ||||||
| chr1:183379092
|
A | ATCTATAT others(10): Show |
4 | a0001c0001t0004g0054a0001c0001t0016g0253a0001c0001t0078g0043others(1): Show | 4 | HG00140.hp2 HG02074.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+39090_85+39091i others(19): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379092 | ||||||
| chr1:183379092
|
A | ATCTATAT others(28): Show |
1 | a0001c0001t0037g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85+39090_85+39091i others(37): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379092 | ||||||
| chr1:183379108
|
C | A | 2 | a0001c0001t0004g0178a0001c0001t0094g0248 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.85+39075G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379108 | ||||||
| chr1:183379114
|
C | A | 2 | a0001c0001t0009g0084a0001c0001t0056g0151 | 2 | HG01884.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.85+39069G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379114 | ||||||
| chr1:183379116
|
C | A | 90 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(87): Show | 90 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+39067G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379116 | ||||||
| chr1:183379117
|
T | C | 71 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.85+39066A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379117 | ||||||
| chr1:183379258
|
G | A | 25 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(22): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+38925C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379258 | ||||||
| chr1:183379276
|
G | A | 23 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0002g0049others(20): Show | 23 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+38907C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379276 | ||||||
| chr1:183379342
|
A | G | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.85+38841T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379342 | ||||||
| chr1:183379386
|
G | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+38797C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379386 | ||||||
| chr1:183379625
|
C | G | 8 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+38558G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379625 | ||||||
| chr1:183379847
|
G | A | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+38336C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379847 | ||||||
| chr1:183379981
|
T | C | 1 | a0001c0001t0081g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.85+38202A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183379981 | ||||||
| chr1:183380422
|
C | T | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+37761G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380422 | ||||||
| chr1:183380622
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.85+37561C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380622 | ||||||
| chr1:183380701
|
T | A | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.85+37482A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380701 | ||||||
| chr1:183380813
|
A | T | 2 | a0001c0001t0006g0098a0001c0001t0018g0111 | 2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.85+37370T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380813 | ||||||
| chr1:183380817
|
C | T | 2 | a0001c0001t0018g0197a0001c0001t0040g0205 | 2 | HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.85+37366G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380817 | ||||||
| chr1:183380892
|
T | C | 1 | a0001c0001t0007g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.85+37291A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380892 | ||||||
| chr1:183380955
|
G | T | 1 | a0001c0001t0024g0099 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.85+37228C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183380955 | ||||||
| chr1:183381048
|
G | A | 1 | a0001c0001t0056g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.85+37135C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183381048 | ||||||
| chr1:183381612
|
G | A | 1 | a0001c0001t0077g0193 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.85+36571C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183381612 | ||||||
| chr1:183381827
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.85+36356A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183381827 | ||||||
| chr1:183381913
|
G | T | 4 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+36270C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183381913 | ||||||
| chr1:183382121
|
A | T | 92 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.85+36062T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382121 | ||||||
| chr1:183382239
|
G | T | 1 | a0001c0001t0012g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.85+35944C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382239 | ||||||
| chr1:183382596
|
G | T | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+35587C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382596 | ||||||
| chr1:183382649
|
T | A | 182 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.85+35534A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382649 | ||||||
| chr1:183382766
|
G | A | 1 | a0001c0001t0014g0073 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.85+35417C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382766 | ||||||
| chr1:183382908
|
C | T | 1 | a0001c0003t0015g0224 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.85+35275G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382908 | ||||||
| chr1:183382916
|
T | C | 90 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(87): Show | 90 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+35267A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183382916 | ||||||
| chr1:183383112
|
G | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+35071C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383112 | ||||||
| chr1:183383128
|
G | A | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+35055C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383128 | ||||||
| chr1:183383304
|
G | A | 18 | a0001c0001t0002g0158a0001c0001t0002g0164a0001c0001t0003g0156others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+34879C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383304 | ||||||
| chr1:183383308
|
C | T | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+34875G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383308 | ||||||
| chr1:183383430
|
G | A | 83 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(80): Show | 83 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.85+34753C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383430 | ||||||
| chr1:183383441
|
C | T | 7 | a0001c0001t0016g0175a0001c0001t0017g0171a0001c0001t0017g0173others(4): Show | 7 | HG01109.hp2 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+34742G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383441 | ||||||
| chr1:183383501
|
GC | G | 35 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(32): Show | 35 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.85+34681delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383501 | ||||||
| chr1:183383510
|
C | A | 3 | a0001c0001t0062g0225a0001c0001t0081g0200a0001c0001t0086g0206 | 3 | HG03239.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.85+34673G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383510 | ||||||
| chr1:183383609
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+34574C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383609 | ||||||
| chr1:183383728
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.85+34455G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383728 | ||||||
| chr1:183383859
|
C | T | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+34324G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383859 | ||||||
| chr1:183383883
|
G | A | 1 | a0001c0001t0016g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.85+34300C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383883 | ||||||
| chr1:183383938
|
A | G | 30 | a0001c0001t0001g0101a0001c0001t0004g0006a0001c0001t0005g0005others(27): Show | 30 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.85+34245T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183383938 | ||||||
| chr1:183384006
|
A | T | 6 | a0001c0001t0005g0239a0001c0001t0011g0015a0001c0001t0025g0014others(3): Show | 6 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+34177T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384006 | ||||||
| chr1:183384029
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85+34154T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384029 | ||||||
| chr1:183384048
|
A | C | 83 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(80): Show | 83 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.85+34135T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384048 | ||||||
| chr1:183384053
|
G | A | 3 | a0001c0001t0017g0002a0001c0001t0090g0226a0001c0001t0092g0003 | 3 | HG02280.hp2 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.85+34130C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384053 | ||||||
| chr1:183384196
|
A | ACACTTTT others(265): Show |
2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+33986_85+33987i others(274): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384196 | ||||||
| chr1:183384196
|
A | ACACTTTT others(268): Show |
5 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(2): Show | 5 | HG02809.hp1 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+33986_85+33987i others(277): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384196 | ||||||
| chr1:183384423
|
C | G | 1 | a0001c0001t0002g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.85+33760G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384423 | ||||||
| chr1:183384533
|
AACTC | A | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+33646_85+33649d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384533 | ||||||
| chr1:183384543
|
C | T | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+33640G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384543 | ||||||
| chr1:183384595
|
C | T | 182 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(179): Show | 182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.85+33588G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384595 | ||||||
| chr1:183384603
|
C | T | 1 | a0001c0001t0034g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.85+33580G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384603 | ||||||
| chr1:183384634
|
C | A | 18 | a0001c0001t0002g0158a0001c0001t0002g0164a0001c0001t0003g0156others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+33549G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384634 | ||||||
| chr1:183384666
|
C | A | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85+33517G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384666 | ||||||
| chr1:183384718
|
C | T | 90 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.85+33465G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384718 | ||||||
| chr1:183384798
|
T | G | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+33385A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384798 | ||||||
| chr1:183384852
|
T | C | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+33331A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384852 | ||||||
| chr1:183384931
|
TCTGTAGT others(4): Show |
T | 1 | a0001c0001t0013g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85+33241_85+33251d others(13): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183384931 | ||||||
| chr1:183385202
|
TA | T | 5 | a0001c0001t0016g0253a0001c0001t0016g0254a0001c0001t0016g0256others(2): Show | 5 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+32980delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183385202 | ||||||
| chr1:183385953
|
C | T | 19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+32230G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183385953 | ||||||
| chr1:183386062
|
G | A | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+32121C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386062 | ||||||
| chr1:183386244
|
T | G | 1 | a0001c0001t0022g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.85+31939A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386244 | ||||||
| chr1:183386397
|
G | A | 7 | a0001c0001t0016g0175a0001c0001t0017g0171a0001c0001t0017g0173others(4): Show | 7 | HG01109.hp2 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+31786C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386397 | ||||||
| chr1:183386399
|
A | G | 4 | a0001c0001t0014g0070a0001c0001t0014g0071a0001c0001t0014g0072others(1): Show | 4 | NA18968.hp2 NA18983.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+31784T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386399 | ||||||
| chr1:183386529
|
A | C | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+31654T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386529 | ||||||
| chr1:183386567
|
C | G | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+31616G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386567 | ||||||
| chr1:183386567
|
C | T | 5 | a0001c0001t0005g0239a0001c0001t0011g0015a0001c0001t0025g0014others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+31616G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386567 | ||||||
| chr1:183386619
|
G | T | 5 | a0001c0001t0005g0239a0001c0001t0011g0015a0001c0001t0025g0014others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+31564C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386619 | ||||||
| chr1:183386729
|
T | G | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.85+31454A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386729 | ||||||
| chr1:183386741
|
T | C | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+31442A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183386741 | ||||||
| chr1:183387199
|
A | ACAGCTCT others(4): Show |
1 | a0001c0001t0013g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85+30973_85+30983d others(13): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387199 | ||||||
| chr1:183387239
|
G | GT | 77 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(74): Show | 77 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.85+30943dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387239 | ||||||
| chr1:183387239
|
GT | G | 23 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.85+30943delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387239 | ||||||
| chr1:183387343
|
A | C | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+30840T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387343 | ||||||
| chr1:183387388
|
G | A | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+30795C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387388 | ||||||
| chr1:183387559
|
T | C | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+30624A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387559 | ||||||
| chr1:183387602
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.85+30581C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387602 | ||||||
| chr1:183387796
|
G | A | 79 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(76): Show | 79 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.85+30387C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183387796 | ||||||
| chr1:183388208
|
G | A | 3 | a0001c0001t0002g0086a0001c0001t0032g0184a0001c0001t0089g0085 | 3 | HG01123.hp2 HG01192.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.85+29975C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388208 | ||||||
| chr1:183388236
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+29947C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388236 | ||||||
| chr1:183388270
|
G | C | 1 | a0001c0001t0046g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.85+29913C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388270 | ||||||
| chr1:183388293
|
G | GA | 24 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(21): Show | 24 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.85+29889dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388293 | ||||||
| chr1:183388319
|
C | T | 2 | a0001c0001t0032g0184a0001c0001t0089g0085 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85+29864G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388319 | ||||||
| chr1:183388428
|
G | T | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+29755C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388428 | ||||||
| chr1:183388525
|
A | G | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+29658T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388525 | ||||||
| chr1:183388634
|
A | G | 3 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0019g0191 | 3 | HG00280.hp1 HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.85+29549T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388634 | ||||||
| chr1:183388682
|
C | T | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+29501G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388682 | ||||||
| chr1:183388686
|
T | A | 20 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.85+29497A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183388686 | ||||||
| chr1:183389034
|
T | C | 25 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(22): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+29149A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389034 | ||||||
| chr1:183389128
|
C | G | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+29055G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389128 | ||||||
| chr1:183389270
|
C | T | 81 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(78): Show | 81 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.85+28913G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389270 | ||||||
| chr1:183389305
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.85+28878A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389305 | ||||||
| chr1:183389466
|
C | A | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+28717G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389466 | ||||||
| chr1:183389734
|
AAAAAAGA others(15): Show |
A | 1 | a0001c0001t0012g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.85+28427_85+28448d others(24): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389734 | ||||||
| chr1:183389734
|
AAAAAAGA others(19): Show |
A | 1 | a0001c0001t0006g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.85+28423_85+28448d others(28): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389734 | ||||||
| chr1:183389735
|
AAAAAGAA others(6): Show |
A | 3 | a0001c0001t0003g0187a0001c0001t0008g0135a0001c0001t0040g0094 | 3 | HG00099.hp1 HG00140.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.85+28435_85+28447d others(15): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389735 | ||||||
| chr1:183389735
|
AAAAAGAA others(10): Show |
A | 2 | a0001c0001t0002g0082a0001c0001t0032g0108 | 2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+28431_85+28447d others(19): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389735 | ||||||
| chr1:183389736
|
A | AAAAG | 7 | a0001c0001t0002g0199a0001c0001t0007g0183a0001c0001t0009g0084others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+28443_85+28446d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
A | AAAAGAAA others(1): Show |
6 | a0001c0001t0001g0142a0001c0001t0009g0120a0001c0001t0013g0129others(3): Show | 6 | HG02451.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+28439_85+28446d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
A | AAAAGAAA others(5): Show |
4 | a0001c0001t0001g0124a0001c0001t0003g0201a0001c0001t0004g0178others(1): Show | 4 | HG02155.hp1 HG02273.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+28435_85+28446d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAG | A | 19 | a0001c0001t0001g0132a0001c0001t0004g0168a0001c0001t0005g0104others(16): Show | 19 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+28443_85+28446d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(1): Show |
A | 17 | a0001c0001t0002g0164a0001c0001t0002g0210a0001c0001t0003g0163others(14): Show | 17 | HG00423.hp2 HG00438.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.85+28439_85+28446d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(5): Show |
A | 21 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0137others(18): Show | 21 | HG01081.hp1 HG01123.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.85+28435_85+28446d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(9): Show |
A | 10 | a0001c0001t0001g0245a0001c0001t0002g0001a0001c0001t0003g0160others(7): Show | 11 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+28431_85+28446d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(13): Show |
A | 25 | a0001c0001t0001g0128a0001c0001t0001g0243a0001c0001t0002g0037others(22): Show | 25 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.85+28427_85+28446d others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(17): Show |
A | 12 | a0001c0001t0001g0140a0001c0001t0004g0152a0001c0001t0006g0195others(9): Show | 12 | HG00738.hp1 HG01099.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.85+28423_85+28446d others(26): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(21): Show |
A | 14 | a0001c0001t0001g0101a0001c0001t0002g0219a0001c0001t0003g0217others(11): Show | 14 | HG00735.hp1 HG01167.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+28419_85+28446d others(30): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(25): Show |
A | 3 | a0001c0001t0009g0220a0001c0001t0048g0174a0001c0001t0085g0198 | 3 | HG02280.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.85+28415_85+28446d others(34): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(29): Show |
A | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0022g0240others(1): Show | 4 | HG01346.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+28411_85+28446d others(38): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(33): Show |
A | 4 | a0001c0001t0016g0194a0001c0001t0032g0184a0001c0001t0089g0085others(1): Show | 4 | HG01123.hp2 HG01192.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+28407_85+28446d others(42): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(37): Show |
A | 2 | a0001c0001t0034g0091a0001c0001t0038g0190 | 2 | HG04184.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.85+28403_85+28446d others(46): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(41): Show |
A | 1 | a0001c0001t0033g0110 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.85+28399_85+28446d others(50): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389736
|
AAAAGAAA others(45): Show |
A | 1 | a0001c0001t0002g0086 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85+28395_85+28446d others(54): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389736 | ||||||
| chr1:183389741
|
A | G | 1 | a0001c0001t0010g0066 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.85+28442T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389741 | ||||||
| chr1:183389758
|
A | G | 2 | a0001c0001t0004g0168a0001c0001t0018g0167 | 2 | HG00280.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.85+28425T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389758 | ||||||
| chr1:183389762
|
A | G | 6 | a0001c0001t0002g0164a0001c0001t0003g0163a0001c0001t0003g0165others(3): Show | 6 | HG01169.hp2 HG01192.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+28421T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389762 | ||||||
| chr1:183389766
|
A | G | 2 | a0001c0001t0035g0161a0001c0001t0067g0123 | 2 | HG01167.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.85+28417T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389766 | ||||||
| chr1:183389770
|
A | G | 2 | a0001c0001t0003g0160a0001c0001t0026g0117 | 2 | HG01358.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.85+28413T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389770 | ||||||
| chr1:183389774
|
A | G | 7 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0003g0156others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+28409T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389774 | ||||||
| chr1:183389778
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.85+28405T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389778 | ||||||
| chr1:183389785
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.85+28398T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389785 | ||||||
| chr1:183389786
|
AAGAAAGA others(59): Show |
A | 3 | a0001c0001t0001g0036a0001c0001t0035g0031a0001c0001t0039g0050 | 3 | HG01169.hp1 HG01978.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.85+28331_85+28396d others(68): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389786 | ||||||
| chr1:183389791
|
A | G | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85+28392T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389791 | ||||||
| chr1:183389793
|
A | G | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85+28390T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389793 | ||||||
| chr1:183389794
|
AAGAAAGA others(51): Show |
A | 2 | a0001c0001t0003g0046a0001c0001t0013g0067 | 2 | HG00438.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.85+28331_85+28388d others(60): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389794 | ||||||
| chr1:183389795
|
A | G | 2 | a0001c0001t0006g0061a0001c0001t0042g0058 | 2 | HG02965.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.85+28388T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389795 | ||||||
| chr1:183389796
|
GAAAGAAA others(48): Show |
G | 1 | a0001c0001t0006g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.85+28332_85+28386d others(57): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389796 | ||||||
| chr1:183389797
|
A | G | 4 | a0001c0001t0005g0077a0001c0001t0012g0059a0001c0001t0014g0072others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28386T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389797 | ||||||
| chr1:183389798
|
AAGAAAGA others(47): Show |
A | 4 | a0001c0001t0001g0045a0001c0001t0002g0049a0001c0001t0007g0069others(1): Show | 4 | HG01070.hp1 HG02523.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28331_85+28384d others(56): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389798 | ||||||
| chr1:183389799
|
A | G | 3 | a0001c0001t0005g0077a0001c0001t0012g0059a0001c0001t0042g0058 | 3 | HG01884.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.85+28384T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389799 | ||||||
| chr1:183389800
|
GAAAGAAA others(44): Show |
G | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+28332_85+28382d others(53): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389800 | ||||||
| chr1:183389801
|
A | G | 2 | a0001c0001t0012g0059a0001c0001t0042g0058 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.85+28382T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389801 | ||||||
| chr1:183389802
|
AAGAAAGA others(43): Show |
A | 3 | a0001c0001t0010g0066a0001c0001t0030g0017a0001c0001t0075g0063 | 3 | HG00609.hp1 HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.85+28331_85+28380d others(52): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389802 | ||||||
| chr1:183389803
|
A | G | 5 | a0001c0001t0003g0030a0001c0001t0010g0057a0001c0001t0012g0059others(2): Show | 5 | HG01258.hp1 HG01258.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+28380T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389803 | ||||||
| chr1:183389804
|
GAAAGAAA others(40): Show |
G | 3 | a0001c0001t0012g0059a0001c0001t0042g0058a0001c0001t0071g0025 | 3 | HG01884.hp2 HG02965.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.85+28332_85+28378d others(49): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389804 | ||||||
| chr1:183389804
|
GAAAGAAA others(42): Show |
G | 1 | a0001c0001t0052g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.85+28330_85+28378d others(51): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389804 | ||||||
| chr1:183389805
|
A | G | 4 | a0001c0001t0003g0030a0001c0001t0010g0057a0001c0001t0012g0080others(1): Show | 4 | HG01258.hp1 HG01258.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28378T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389805 | ||||||
| chr1:183389806
|
AAGAAAGA others(39): Show |
A | 1 | a0001c0001t0003g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.85+28331_85+28376d others(48): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389806 | ||||||
| chr1:183389807
|
A | G | 6 | a0001c0001t0003g0030a0001c0001t0010g0057a0001c0001t0012g0080others(3): Show | 6 | HG01258.hp1 HG01258.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+28376T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389807 | ||||||
| chr1:183389808
|
GAAAGAAA others(36): Show |
G | 1 | a0001c0001t0012g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.85+28332_85+28374d others(45): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389808 | ||||||
| chr1:183389809
|
A | G | 8 | a0001c0001t0003g0030a0001c0001t0004g0054a0001c0001t0005g0055others(5): Show | 8 | HG00140.hp2 HG01258.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+28374T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389809 | ||||||
| chr1:183389809
|
AAAGAAAG others(36): Show |
A | 1 | a0001c0001t0003g0032 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.85+28331_85+28373d others(45): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389809 | ||||||
| chr1:183389811
|
A | G | 13 | a0001c0001t0003g0030a0001c0001t0004g0054a0001c0001t0005g0055others(10): Show | 13 | HG00140.hp2 HG01258.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.85+28372T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389811 | ||||||
| chr1:183389812
|
GAAAGAAA others(14): Show |
G | 1 | a0001c0001t0015g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.85+28350_85+28370d others(23): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389812 | ||||||
| chr1:183389812
|
GAAAGAAA others(30): Show |
G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28334_85+28370d others(39): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389812 | ||||||
| chr1:183389812
|
GAAAGAAA others(32): Show |
G | 4 | a0001c0001t0003g0030a0001c0001t0010g0057a0001c0001t0051g0081others(1): Show | 4 | HG01258.hp1 HG01258.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28332_85+28370d others(41): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389812 | ||||||
| chr1:183389813
|
A | G | 12 | a0001c0001t0003g0029a0001c0001t0004g0054a0001c0001t0005g0055others(9): Show | 12 | HG00140.hp2 HG01975.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.85+28370T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389813 | ||||||
| chr1:183389813
|
AAAGAAAG others(25): Show |
A | 1 | a0001c0001t0093g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.85+28338_85+28369d others(34): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389813 | ||||||
| chr1:183389813
|
AAAGAAAG others(32): Show |
A | 1 | a0001c0001t0003g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.85+28331_85+28369d others(41): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389813 | ||||||
| chr1:183389814
|
A | G | 1 | a0001c0001t0014g0073 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.85+28369T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389814 | ||||||
| chr1:183389814
|
AAGAAAGA others(31): Show |
A | 2 | a0001c0001t0003g0065a0001c0001t0005g0047 | 2 | NA18977.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.85+28331_85+28368d others(40): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389814 | ||||||
| chr1:183389815
|
A | G | 16 | a0001c0001t0003g0029a0001c0001t0004g0054a0001c0001t0005g0055others(13): Show | 16 | HG00140.hp2 HG01975.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.85+28368T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389815 | ||||||
| chr1:183389816
|
G | T | 2 | a0001c0001t0018g0197a0001c0001t0040g0205 | 2 | HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.85+28367C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389816 | ||||||
| chr1:183389816
|
GAAAGAAA others(28): Show |
G | 2 | a0001c0001t0008g0042a0001c0001t0009g0078 | 2 | HG03834.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.85+28332_85+28366d others(37): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389816 | ||||||
| chr1:183389817
|
A | G | 16 | a0001c0001t0003g0029a0001c0001t0004g0054a0001c0001t0005g0055others(13): Show | 16 | HG00140.hp2 HG01106.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.85+28366T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389817 | ||||||
| chr1:183389817
|
AAAGAAAG others(20): Show |
A | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.85+28339_85+28365d others(29): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389817 | ||||||
| chr1:183389817
|
AAAGAAAG others(28): Show |
A | 1 | a0001c0001t0014g0073 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.85+28331_85+28365d others(37): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389817 | ||||||
| chr1:183389819
|
A | G | 17 | a0001c0001t0002g0013a0001c0001t0003g0029a0001c0001t0004g0054others(14): Show | 17 | HG00140.hp2 HG01106.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.85+28364T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389819 | ||||||
| chr1:183389820
|
GAAAGAAA others(14): Show |
G | 1 | a0001c0001t0045g0146 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.85+28342_85+28362d others(23): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389820 | ||||||
| chr1:183389820
|
GAAAGAAA others(21): Show |
G | 1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85+28335_85+28362d others(30): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389820 | ||||||
| chr1:183389820
|
GAAAGAAA others(24): Show |
G | 5 | a0001c0001t0004g0054a0001c0001t0005g0055a0001c0001t0014g0071others(2): Show | 5 | HG00140.hp2 HG04115.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+28332_85+28362d others(33): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389820 | ||||||
| chr1:183389821
|
A | G | 17 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0003g0029others(14): Show | 17 | HG00609.hp2 HG01106.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.85+28362T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389821 | ||||||
| chr1:183389822
|
A | G | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.85+28361T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389822 | ||||||
| chr1:183389823
|
A | G | 16 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0003g0029others(13): Show | 16 | HG00609.hp2 HG01106.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.85+28360T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389823 | ||||||
| chr1:183389823
|
AGAAAGAA others(14): Show |
A | 1 | a0001c0001t0018g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.85+28339_85+28359d others(23): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389823 | ||||||
| chr1:183389824
|
GAAAGAAA others(20): Show |
G | 8 | a0001c0001t0003g0029a0001c0001t0012g0039a0001c0001t0014g0070others(5): Show | 8 | HG01975.hp2 HG02486.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+28332_85+28358d others(29): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389824 | ||||||
| chr1:183389824
|
GAAAGAAA others(22): Show |
G | 1 | a0001c0001t0004g0044 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.85+28330_85+28358d others(31): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389824 | ||||||
| chr1:183389825
|
A | G | 11 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(8): Show | 11 | HG00609.hp2 HG01106.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.85+28358T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389825 | ||||||
| chr1:183389827
|
A | G | 13 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(10): Show | 13 | HG00609.hp2 HG01106.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.85+28356T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389827 | ||||||
| chr1:183389829
|
A | G | 15 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(12): Show | 15 | HG00609.hp2 HG01106.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+28354T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389829 | ||||||
| chr1:183389831
|
A | G | 16 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(13): Show | 16 | HG00609.hp2 HG01106.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.85+28352T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389831 | ||||||
| chr1:183389833
|
A | G | 18 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(15): Show | 18 | HG00609.hp2 HG01106.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+28350T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389833 | ||||||
| chr1:183389835
|
A | G | 20 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(17): Show | 20 | HG00609.hp2 HG01106.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.85+28348T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389835 | ||||||
| chr1:183389837
|
A | G | 24 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0250others(21): Show | 24 | HG00609.hp2 HG01069.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.85+28346T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389837 | ||||||
| chr1:183389839
|
A | G | 23 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0250others(20): Show | 23 | HG00609.hp2 HG01106.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+28344T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389839 | ||||||
| chr1:183389841
|
A | G | 27 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0250others(24): Show | 27 | HG00609.hp2 HG01069.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.85+28342T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389841 | ||||||
| chr1:183389842
|
A | G | 1 | a0001c0001t0010g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.85+28341T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389842 | ||||||
| chr1:183389843
|
A | G | 23 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0002g0250others(20): Show | 23 | HG00609.hp2 HG01106.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+28340T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389843 | ||||||
| chr1:183389845
|
G | A | 1 | a0001c0001t0013g0090 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.85+28338C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389845
|
GAAAAAAG others(3): Show |
G | 4 | a0001c0001t0010g0009a0001c0001t0020g0247a0001c0001t0028g0255others(1): Show | 4 | HG01952.hp2 HG01981.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28328_85+28337d others(12): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389845
|
GAAAAAAG others(7): Show |
G | 5 | a0001c0001t0016g0254a0001c0001t0016g0256a0001c0001t0037g0252others(2): Show | 5 | HG01993.hp1 HG02723.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+28324_85+28337d others(16): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389845
|
GAAAAAAG others(11): Show |
G | 2 | a0001c0001t0043g0074a0001c0001t0080g0053 | 2 | HG00609.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.85+28320_85+28337d others(20): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389845
|
GAAAAAAG others(15): Show |
G | 4 | a0001c0001t0016g0253a0001c0001t0019g0052a0001c0001t0047g0075others(1): Show | 4 | HG02109.hp1 NA19007.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28316_85+28337d others(24): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389845
|
GAAAAAAG others(19): Show |
G | 5 | a0001c0001t0002g0013a0001c0001t0002g0041a0001c0001t0005g0076others(2): Show | 5 | HG01106.hp2 HG02074.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+28312_85+28337d others(28): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389845 | ||||||
| chr1:183389846
|
A | G | 1 | a0001c0001t0010g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.85+28337T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389846 | ||||||
| chr1:183389847
|
A | G | 1 | a0001c0001t0002g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.85+28336T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389847 | ||||||
| chr1:183389848
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0010g0011others(1): Show | 4 | HG02148.hp2 HG03195.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+28335T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389848 | ||||||
| chr1:183389849
|
A | G | 2 | a0001c0001t0002g0250a0001c0001t0010g0011 | 2 | HG02148.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.85+28334T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389849 | ||||||
| chr1:183389850
|
A | G | 1 | a0001c0001t0010g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.85+28333T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389850 | ||||||
| chr1:183389851
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.85+28332T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389851 | ||||||
| chr1:183389853
|
A | G | 7 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0005g0047others(4): Show | 7 | HG01257.hp2 HG02148.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+28330T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389853 | ||||||
| chr1:183389854
|
GAAA | G | 26 | a0001c0001t0001g0035a0001c0001t0003g0029a0001c0001t0003g0030others(23): Show | 26 | HG00140.hp2 HG01258.hp1 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+28326_85+28328d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389854 | ||||||
| chr1:183389855
|
A | G | 7 | a0001c0001t0002g0250a0001c0001t0003g0032a0001c0001t0004g0044others(4): Show | 7 | HG01257.hp2 HG02717.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+28328T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389855 | ||||||
| chr1:183389856
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28327T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389856 | ||||||
| chr1:183389857
|
A | G | 15 | a0001c0001t0002g0250a0001c0001t0003g0064a0001c0001t0004g0044others(12): Show | 15 | HG01257.hp2 HG01952.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+28326T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389857 | ||||||
| chr1:183389859
|
A | G | 41 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(38): Show | 41 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.85+28324T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389859 | ||||||
| chr1:183389860
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28323T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389860 | ||||||
| chr1:183389861
|
A | G | 47 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(44): Show | 47 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(44): Show |
intron_variant | MODIFIER | c.85+28322T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389861 | ||||||
| chr1:183389863
|
A | G | 46 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(43): Show | 46 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.85+28320T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389863 | ||||||
| chr1:183389864
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28319T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389864 | ||||||
| chr1:183389865
|
A | G | 49 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(46): Show | 49 | HG00140.hp2 HG00609.hp2 HG01257.hp2 others(46): Show |
intron_variant | MODIFIER | c.85+28318T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389865 | ||||||
| chr1:183389867
|
A | G | 48 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(45): Show | 48 | HG00140.hp2 HG00609.hp2 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.85+28316T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389867 | ||||||
| chr1:183389868
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28315T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389868 | ||||||
| chr1:183389869
|
A | G | 53 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(50): Show | 53 | HG00140.hp2 HG00609.hp2 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.85+28314T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389869 | ||||||
| chr1:183389871
|
A | AAGGG | 35 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(32): Show | 35 | HG00140.hp1 HG00738.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.85+28308_85+28311d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
A | AAGGGAGG others(1): Show |
6 | a0001c0001t0017g0171a0001c0001t0017g0173a0001c0001t0017g0176others(3): Show | 6 | HG01109.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+28304_85+28311d others(10): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
A | AAGGGAGG others(5): Show |
2 | a0001c0001t0030g0017a0001c0001t0060g0048 | 2 | NA18946.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.85+28300_85+28311d others(14): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
A | AAGGGAGG others(9): Show |
9 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0002g0049others(6): Show | 9 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+28296_85+28311d others(18): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
A | AAGGGAGG others(13): Show |
2 | a0001c0001t0003g0062a0001c0001t0075g0063 | 2 | HG00609.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.85+28292_85+28311d others(22): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
A | G | 52 | a0001c0001t0001g0035a0001c0001t0002g0250a0001c0001t0003g0029others(49): Show | 52 | HG00140.hp2 HG00609.hp2 HG01257.hp2 others(49): Show |
intron_variant | MODIFIER | c.85+28312T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389871
|
AAGGG | A | 4 | a0001c0001t0062g0225a0001c0001t0066g0116a0001c0001t0079g0177others(1): Show | 4 | HG02451.hp1 HG03209.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+28308_85+28311d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389871 | ||||||
| chr1:183389872
|
A | G | 1 | a0001c0001t0038g0079 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.85+28311T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389872 | ||||||
| chr1:183389897
|
G | GGGAA | 3 | a0001c0001t0017g0002a0001c0001t0090g0226a0001c0001t0092g0003 | 3 | HG02280.hp2 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.85+28282_85+28285d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389897 | ||||||
| chr1:183389901
|
A | G | 1 | a0001c0001t0028g0255 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.85+28282T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183389901 | ||||||
| chr1:183390026
|
C | T | 1 | a0001c0001t0015g0204 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.85+28157G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390026 | ||||||
| chr1:183390329
|
A | T | 2 | a0001c0001t0032g0184a0001c0001t0089g0085 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85+27854T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390329 | ||||||
| chr1:183390331
|
A | T | 2 | a0001c0001t0032g0184a0001c0001t0089g0085 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85+27852T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390331 | ||||||
| chr1:183390379
|
C | T | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+27804G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390379 | ||||||
| chr1:183390744
|
C | T | 35 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(32): Show | 35 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.85+27439G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390744 | ||||||
| chr1:183390787
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85+27396C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390787 | ||||||
| chr1:183390918
|
G | C | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.85+27265C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390918 | ||||||
| chr1:183390921
|
G | A | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+27262C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390921 | ||||||
| chr1:183390942
|
C | A | 1 | a0001c0001t0039g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.85+27241G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183390942 | ||||||
| chr1:183391160
|
C | A | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+27023G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391160 | ||||||
| chr1:183391272
|
T | A | 1 | a0001c0001t0050g0018 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.85+26911A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391272 | ||||||
| chr1:183391326
|
T | C | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+26857A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391326 | ||||||
| chr1:183391340
|
T | G | 19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+26843A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391340 | ||||||
| chr1:183391430
|
T | G | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+26753A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391430 | ||||||
| chr1:183391531
|
T | TA | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+26651dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391531 | ||||||
| chr1:183391722
|
G | A | 1 | a0001c0001t0021g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85+26461C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391722 | ||||||
| chr1:183391831
|
C | A | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.85+26352G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391831 | ||||||
| chr1:183391890
|
T | A | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+26293A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391890 | ||||||
| chr1:183391931
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+26252G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391931 | ||||||
| chr1:183391959
|
T | A | 2 | a0001c0001t0034g0091a0001c0001t0070g0113 | 2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.85+26224A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391959 | ||||||
| chr1:183391962
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+26221G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183391962 | ||||||
| chr1:183392000
|
A | G | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+26183T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392000 | ||||||
| chr1:183392143
|
A | G | 2 | a0001c0001t0024g0087a0001c0001t0024g0099 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.85+26040T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392143 | ||||||
| chr1:183392173
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.85+26010G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392173 | ||||||
| chr1:183392412
|
C | T | 1 | a0001c0001t0015g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.85+25771G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392412 | ||||||
| chr1:183392413
|
G | A | 4 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0019g0191others(1): Show | 4 | HG00280.hp1 HG00438.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+25770C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392413 | ||||||
| chr1:183392443
|
C | T | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+25740G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392443 | ||||||
| chr1:183392673
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+25510C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392673 | ||||||
| chr1:183392860
|
C | G | 4 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+25323G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392860 | ||||||
| chr1:183392915
|
G | A | 1 | a0001c0001t0051g0081 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85+25268C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183392915 | ||||||
| chr1:183393039
|
G | A | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+25144C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393039 | ||||||
| chr1:183393062
|
G | A | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+25121C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393062 | ||||||
| chr1:183393105
|
C | T | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+25078G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393105 | ||||||
| chr1:183393131
|
C | G | 1 | a0001c0001t0007g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.85+25052G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393131 | ||||||
| chr1:183393198
|
A | G | 1 | a0001c0001t0076g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.85+24985T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393198 | ||||||
| chr1:183393409
|
G | A | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(73): Show | 76 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.85+24774C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393409 | ||||||
| chr1:183393476
|
T | TA | 30 | a0001c0001t0002g0013a0001c0001t0002g0153a0001c0001t0002g0158others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.85+24706dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393476 | ||||||
| chr1:183393511
|
C | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(68): Show | 71 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.85+24672G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393511 | ||||||
| chr1:183393517
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.85+24666A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393517 | ||||||
| chr1:183393582
|
A | C | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+24601T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393582 | ||||||
| chr1:183393658
|
C | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+24525G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393658 | ||||||
| chr1:183393712
|
C | T | 17 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.85+24471G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393712 | ||||||
| chr1:183393777
|
A | G | 1 | a0001c0001t0080g0053 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.85+24406T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183393777 | ||||||
| chr1:183394117
|
A | G | 1 | a0001c0001t0006g0007 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85+24066T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394117 | ||||||
| chr1:183394125
|
T | C | 1 | a0001c0001t0057g0249 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.85+24058A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394125 | ||||||
| chr1:183394171
|
G | A | 1 | a0001c0001t0006g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.85+24012C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394171 | ||||||
| chr1:183394393
|
C | T | 2 | a0001c0001t0017g0002a0001c0001t0092g0003 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.85+23790G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394393 | ||||||
| chr1:183394654
|
C | T | 1 | a0001c0001t0067g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.85+23529G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394654 | ||||||
| chr1:183394881
|
A | T | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+23302T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394881 | ||||||
| chr1:183394961
|
T | C | 1 | a0001c0001t0005g0239 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.85+23222A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183394961 | ||||||
| chr1:183395143
|
G | A | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+23040C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395143 | ||||||
| chr1:183395225
|
T | G | 4 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+22958A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395225 | ||||||
| chr1:183395248
|
T | C | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+22935A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395248 | ||||||
| chr1:183395280
|
A | C | 2 | a0001c0001t0004g0178a0001c0001t0042g0179 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.85+22903T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395280 | ||||||
| chr1:183395386
|
G | A | 1 | a0001c0001t0041g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.85+22797C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395386 | ||||||
| chr1:183395445
|
G | A | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+22738C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395445 | ||||||
| chr1:183395676
|
G | T | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+22507C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395676 | ||||||
| chr1:183395739
|
T | A | 1 | a0001c0001t0018g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.85+22444A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395739 | ||||||
| chr1:183395896
|
G | A | 1 | a0001c0001t0010g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.85+22287C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183395896 | ||||||
| chr1:183396101
|
G | C | 1 | a0001c0001t0012g0080 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.85+22082C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396101 | ||||||
| chr1:183396305
|
G | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+21878C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396305 | ||||||
| chr1:183396412
|
G | A | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+21771C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396412 | ||||||
| chr1:183396435
|
T | C | 3 | a0001c0001t0009g0078a0001c0001t0012g0080a0001c0001t0038g0079 | 3 | NA18975.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.85+21748A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396435 | ||||||
| chr1:183396560
|
A | G | 2 | a0001c0001t0024g0087a0001c0001t0024g0099 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.85+21623T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396560 | ||||||
| chr1:183396618
|
A | T | 2 | a0001c0001t0006g0202a0001c0001t0006g0203 | 2 | NA18970.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.85+21565T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396618 | ||||||
| chr1:183396738
|
C | T | 1 | a0001c0001t0003g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85+21445G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183396738 | ||||||
| chr1:183397275
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+20908G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397275 | ||||||
| chr1:183397333
|
C | T | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+20850G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397333 | ||||||
| chr1:183397411
|
T | C | 2 | a0001c0001t0032g0184a0001c0001t0089g0085 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85+20772A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397411 | ||||||
| chr1:183397624
|
T | G | 1 | a0001c0001t0009g0120 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.85+20559A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397624 | ||||||
| chr1:183397741
|
G | T | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+20442C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397741 | ||||||
| chr1:183397774
|
G | A | 4 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+20409C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397774 | ||||||
| chr1:183397779
|
T | G | 1 | a0001c0001t0002g0086 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85+20404A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397779 | ||||||
| chr1:183397784
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+20399G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397784 | ||||||
| chr1:183397785
|
G | C | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+20398C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397785 | ||||||
| chr1:183397815
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.85+20368A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183397815 | ||||||
| chr1:183398077
|
A | T | 1 | a0001c0001t0019g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.85+20106T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398077 | ||||||
| chr1:183398128
|
G | A | 3 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.85+20055C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398128 | ||||||
| chr1:183398320
|
G | T | 1 | a0001c0002t0003g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.85+19863C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398320 | ||||||
| chr1:183398604
|
A | G | 1 | a0001c0001t0022g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+19579T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398604 | ||||||
| chr1:183398764
|
A | G | 7 | a0001c0001t0016g0175a0001c0001t0017g0171a0001c0001t0017g0173others(4): Show | 7 | HG01109.hp2 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+19419T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398764 | ||||||
| chr1:183398872
|
A | C | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+19311T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398872 | ||||||
| chr1:183398923
|
G | A | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+19260C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398923 | ||||||
| chr1:183398935
|
A | C | 1 | a0001c0001t0007g0021 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.85+19248T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398935 | ||||||
| chr1:183398994
|
T | A | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+19189A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183398994 | ||||||
| chr1:183399096
|
A | C | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+19087T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399096 | ||||||
| chr1:183399168
|
G | A | 1 | a0001c0001t0015g0238 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.85+19015C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399168 | ||||||
| chr1:183399201
|
C | CAGAATCA others(21): Show |
19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+18981_85+18982i others(30): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399201 | ||||||
| chr1:183399205
|
C | A | 19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+18978G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399205 | ||||||
| chr1:183399206
|
G | T | 19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+18977C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399206 | ||||||
| chr1:183399429
|
C | T | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+18754G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399429 | ||||||
| chr1:183399478
|
A | C | 1 | a0001c0001t0029g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.85+18705T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399478 | ||||||
| chr1:183399724
|
T | G | 2 | a0001c0001t0016g0175a0001c0001t0030g0169 | 2 | HG01109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.85+18459A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399724 | ||||||
| chr1:183399755
|
A | G | 1 | a0001c0001t0025g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.85+18428T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399755 | ||||||
| chr1:183399781
|
T | C | 191 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.85+18402A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399781 | ||||||
| chr1:183399901
|
C | T | 76 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(73): Show | 76 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.85+18282G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399901 | ||||||
| chr1:183399930
|
T | G | 101 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.85+18253A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183399930 | ||||||
| chr1:183400018
|
A | T | 19 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.85+18165T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400018 | ||||||
| chr1:183400115
|
G | A | 70 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(67): Show | 70 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.85+18068C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400115 | ||||||
| chr1:183400174
|
A | T | 1 | a0001c0001t0052g0051 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.85+18009T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400174 | ||||||
| chr1:183400325
|
A | C | 171 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.85+17858T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400325 | ||||||
| chr1:183400567
|
A | G | 1 | a0001c0001t0061g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.85+17616T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400567 | ||||||
| chr1:183400644
|
T | C | 171 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.85+17539A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400644 | ||||||
| chr1:183400645
|
G | A | 171 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.85+17538C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400645 | ||||||
| chr1:183400684
|
C | G | 7 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(4): Show | 7 | HG00738.hp2 HG01952.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+17499G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400684 | ||||||
| chr1:183400761
|
A | G | 1 | a0001c0001t0081g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.85+17422T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400761 | ||||||
| chr1:183400922
|
A | T | 70 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(67): Show | 70 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.85+17261T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400922 | ||||||
| chr1:183400930
|
C | G | 1 | a0001c0001t0017g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.85+17253G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183400930 | ||||||
| chr1:183401236
|
C | T | 3 | a0001c0001t0002g0082a0001c0001t0021g0145a0001c0001t0033g0246 | 3 | HG01891.hp2 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.85+16947G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401236 | ||||||
| chr1:183401314
|
A | T | 1 | a0001c0001t0004g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85+16869T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401314 | ||||||
| chr1:183401523
|
T | C | 1 | a0001c0002t0041g0230 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.85+16660A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401523 | ||||||
| chr1:183401637
|
T | TCA | 5 | a0001c0001t0005g0239a0001c0001t0011g0015a0001c0001t0025g0014others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+16544_85+16545d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401637 | ||||||
| chr1:183401775
|
A | C | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+16408T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401775 | ||||||
| chr1:183401848
|
A | C | 1 | a0001c0001t0004g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.85+16335T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401848 | ||||||
| chr1:183401975
|
C | A | 1 | a0001c0001t0036g0231 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.85+16208G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183401975 | ||||||
| chr1:183402044
|
A | C | 8 | a0001c0001t0005g0104a0001c0001t0005g0112a0001c0001t0011g0103others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+16139T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402044 | ||||||
| chr1:183402057
|
C | A | 78 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(75): Show | 78 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.85+16126G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402057 | ||||||
| chr1:183402069
|
TA | T | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+16113delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402069 | ||||||
| chr1:183402137
|
C | G | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+16046G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402137 | ||||||
| chr1:183402182
|
T | C | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+16001A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402182 | ||||||
| chr1:183402627
|
A | C | 6 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(3): Show | 6 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+15556T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402627 | ||||||
| chr1:183402902
|
AC | A | 170 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.85+15280delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402902 | ||||||
| chr1:183402919
|
C | T | 2 | a0001c0001t0002g0049a0001c0001t0039g0050 | 2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.85+15264G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402919 | ||||||
| chr1:183402960
|
CT | C | 168 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.85+15222delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183402960 | ||||||
| chr1:183403232
|
C | A | 1 | a0001c0002t0003g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.85+14951G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403232 | ||||||
| chr1:183403272
|
A | T | 1 | a0001c0001t0083g0093 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.85+14911T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403272 | ||||||
| chr1:183403440
|
AC | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0082a0001c0001t0002g0086others(81): Show | 85 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.85+14742delG | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403440 | ||||||
| chr1:183403441
|
C | CCCCCCCC others(9871): Show |
1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85+14741_85+14742i others(9880): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403441 | ||||||
| chr1:183403450
|
C | A | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+14733G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403450 | ||||||
| chr1:183403451
|
C | A | 77 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.85+14732G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403451 | ||||||
| chr1:183403462
|
G | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+14721C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403462 | ||||||
| chr1:183403540
|
T | C | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+14643A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403540 | ||||||
| chr1:183403549
|
A | G | 6 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(3): Show | 6 | HG01099.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+14634T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183403549 | ||||||
| chr1:183404099
|
A | AT | 84 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(81): Show | 84 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.85+14083dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404099 | ||||||
| chr1:183404099
|
A | ATT | 53 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(50): Show | 53 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.85+14082_85+14083d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404099 | ||||||
| chr1:183404099
|
A | ATTT | 8 | a0001c0001t0005g0047a0001c0001t0005g0076a0001c0001t0014g0070others(5): Show | 8 | HG02698.hp2 HG03239.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+14081_85+14083d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404099 | ||||||
| chr1:183404099
|
AT | A | 16 | a0001c0001t0002g0082a0001c0001t0007g0019a0001c0001t0007g0020others(13): Show | 16 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.85+14083delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404099 | ||||||
| chr1:183404412
|
A | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+13771T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404412 | ||||||
| chr1:183404530
|
T | C | 177 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.85+13653A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404530 | ||||||
| chr1:183404536
|
A | T | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+13647T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404536 | ||||||
| chr1:183404694
|
C | T | 4 | a0001c0001t0020g0095a0001c0001t0020g0096a0001c0001t0040g0094others(1): Show | 4 | NA18945.hp1 NA18946.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+13489G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404694 | ||||||
| chr1:183404697
|
T | A | 1 | a0001c0001t0008g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.85+13486A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404697 | ||||||
| chr1:183404706
|
A | G | 184 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.85+13477T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404706 | ||||||
| chr1:183404822
|
T | C | 4 | a0001c0001t0014g0070a0001c0001t0014g0071a0001c0001t0014g0072others(1): Show | 4 | NA18968.hp2 NA18983.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+13361A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404822 | ||||||
| chr1:183404880
|
T | C | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.85+13303A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404880 | ||||||
| chr1:183404905
|
A | G | 184 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.85+13278T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404905 | ||||||
| chr1:183404943
|
G | A | 1 | a0001c0001t0017g0176 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.85+13240C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404943 | ||||||
| chr1:183404975
|
C | T | 1 | a0001c0001t0013g0092 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.85+13208G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183404975 | ||||||
| chr1:183405583
|
C | T | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+12600G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183405583 | ||||||
| chr1:183405587
|
C | T | 166 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.85+12596G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183405587 | ||||||
| chr1:183405703
|
T | G | 18 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+12480A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183405703 | ||||||
| chr1:183405831
|
C | T | 1 | a0001c0001t0071g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.85+12352G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183405831 | ||||||
| chr1:183406071
|
T | A | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+12112A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406071 | ||||||
| chr1:183406144
|
A | G | 1 | a0001c0001t0004g0006 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.85+12039T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406144 | ||||||
| chr1:183406159
|
G | T | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+12024C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406159 | ||||||
| chr1:183406176
|
T | C | 193 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.85+12007A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406176 | ||||||
| chr1:183406319
|
G | A | 26 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+11864C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406319 | ||||||
| chr1:183406393
|
G | A | 1 | a0001c0001t0025g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.85+11790C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406393 | ||||||
| chr1:183406466
|
A | G | 193 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.85+11717T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406466 | ||||||
| chr1:183406484
|
C | T | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+11699G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406484 | ||||||
| chr1:183406565
|
T | C | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+11618A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406565 | ||||||
| chr1:183406799
|
T | TGCTCTG | 63 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(60): Show | 63 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.85+11378_85+11383d others(8): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406799 | ||||||
| chr1:183406812
|
C | CT | 7 | a0001c0001t0002g0199a0001c0001t0011g0192a0001c0001t0017g0002others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+11370dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406812 | ||||||
| chr1:183406812
|
CTT | C | 32 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0002g0037others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.85+11369_85+11370d others(4): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406812 | ||||||
| chr1:183406812
|
CTTT | C | 138 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0124others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.85+11368_85+11370d others(5): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406812 | ||||||
| chr1:183406812
|
CTTTT | C | 13 | a0001c0001t0002g0149a0001c0001t0005g0112a0001c0001t0009g0084others(10): Show | 13 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+11367_85+11370d others(6): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406812 | ||||||
| chr1:183406879
|
C | A | 1 | a0001c0001t0043g0074 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85+11304G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183406879 | ||||||
| chr1:183407048
|
A | C | 1 | a0001c0001t0004g0233 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.85+11135T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407048 | ||||||
| chr1:183407106
|
T | A | 8 | a0001c0001t0004g0178a0001c0001t0007g0183a0001c0001t0029g0181others(5): Show | 8 | HG02074.hp1 HG02155.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+11077A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407106 | ||||||
| chr1:183407163
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.85+11020G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407163 | ||||||
| chr1:183407258
|
A | G | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+10925T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407258 | ||||||
| chr1:183407329
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.85+10854G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407329 | ||||||
| chr1:183407467
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.85+10716T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407467 | ||||||
| chr1:183407521
|
A | G | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+10662T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407521 | ||||||
| chr1:183407675
|
T | A | 26 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+10508A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407675 | ||||||
| chr1:183407722
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+10461C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407722 | ||||||
| chr1:183407751
|
A | G | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+10432T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407751 | ||||||
| chr1:183407845
|
G | T | 36 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(33): Show | 36 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.85+10338C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183407845 | ||||||
| chr1:183408092
|
C | T | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+10091G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408092 | ||||||
| chr1:183408203
|
C | T | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+9980G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408203 | ||||||
| chr1:183408538
|
C | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+9645G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408538 | ||||||
| chr1:183408540
|
T | C | 193 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.85+9643A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408540 | ||||||
| chr1:183408825
|
AT | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+9357delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408825 | ||||||
| chr1:183408837
|
A | T | 18 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+9346T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408837 | ||||||
| chr1:183408874
|
A | T | 1 | a0001c0001t0002g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.85+9309T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408874 | ||||||
| chr1:183408916
|
G | A | 81 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(78): Show | 81 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.85+9267C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183408916 | ||||||
| chr1:183409173
|
A | G | 43 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.85+9010T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183409173 | ||||||
| chr1:183409895
|
G | T | 8 | a0001c0001t0002g0149a0001c0001t0009g0144a0001c0001t0021g0083others(5): Show | 8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+8288C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183409895 | ||||||
| chr1:183409994
|
C | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+8189G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183409994 | ||||||
| chr1:183410063
|
C | A | 6 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(3): Show | 6 | HG01099.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+8120G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410063 | ||||||
| chr1:183410084
|
G | A | 2 | a0001c0001t0002g0001a0001c0001t0009g0232 | 3 | HG01069.hp2 HG01071.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.85+8099C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410084 | ||||||
| chr1:183410157
|
C | CA | 20 | a0001c0001t0001g0142a0001c0001t0002g0250a0001c0001t0004g0233others(17): Show | 20 | HG01099.hp1 HG01981.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.85+8025dupT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410157 | ||||||
| chr1:183410157
|
C | CAA | 5 | a0001c0001t0016g0253a0001c0001t0016g0254a0001c0001t0016g0256others(2): Show | 5 | HG02109.hp1 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+8024_85+8025dup others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410157 | ||||||
| chr1:183410157
|
CA | C | 85 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(82): Show | 85 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.85+8025delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410157 | ||||||
| chr1:183410179
|
C | T | 38 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(35): Show | 38 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.85+8004G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410179 | ||||||
| chr1:183410227
|
G | A | 26 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+7956C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410227 | ||||||
| chr1:183410494
|
C | T | 1 | a0001c0001t0044g0196 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+7689G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410494 | ||||||
| chr1:183410580
|
G | A | 1 | a0001c0001t0022g0240 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.85+7603C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410580 | ||||||
| chr1:183410675
|
C | T | 6 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0020g0247others(3): Show | 6 | HG01099.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+7508G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410675 | ||||||
| chr1:183410700
|
A | T | 1 | a0001c0001t0006g0195 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.85+7483T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410700 | ||||||
| chr1:183410737
|
C | CT | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+7445dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410737 | ||||||
| chr1:183410752
|
C | CT | 84 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(81): Show | 84 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.85+7430dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410752 | ||||||
| chr1:183410752
|
C | CTT | 12 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(9): Show | 12 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.85+7429_85+7430dup others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410752 | ||||||
| chr1:183410823
|
T | C | 25 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(22): Show | 25 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.85+7360A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410823 | ||||||
| chr1:183410858
|
C | T | 1 | a0001c0001t0016g0194 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.85+7325G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410858 | ||||||
| chr1:183410891
|
A | T | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.85+7292T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183410891 | ||||||
| chr1:183411009
|
C | T | 2 | a0001c0001t0022g0024a0001c0001t0030g0017 | 2 | HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.85+7174G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411009 | ||||||
| chr1:183411143
|
T | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+7040A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411143 | ||||||
| chr1:183411148
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.85+7035G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411148 | ||||||
| chr1:183411272
|
T | C | 80 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.85+6911A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411272 | ||||||
| chr1:183411458
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+6725G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411458 | ||||||
| chr1:183411476
|
T | G | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.85+6707A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411476 | ||||||
| chr1:183411567
|
T | G | 177 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(174): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.85+6616A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183411567 | ||||||
| chr1:183412129
|
T | G | 5 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(2): Show | 5 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+6054A>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412129 | ||||||
| chr1:183412142
|
G | A | 2 | a0001c0001t0008g0121a0001c0001t0008g0122 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.85+6041C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412142 | ||||||
| chr1:183412175
|
A | G | 2 | a0001c0001t0034g0088a0001c0001t0041g0089 | 2 | HG03017.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.85+6008T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412175 | ||||||
| chr1:183412231
|
G | A | 18 | a0001c0001t0002g0153a0001c0001t0002g0158a0001c0001t0002g0164others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.85+5952C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412231 | ||||||
| chr1:183412246
|
C | T | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.85+5937G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412246 | ||||||
| chr1:183412309
|
C | T | 158 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.85+5874G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412309 | ||||||
| chr1:183412380
|
C | G | 3 | a0001c0001t0008g0121a0001c0001t0008g0122a0001c0001t0061g0118 | 3 | HG01516.hp2 HG01517.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.85+5803G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412380 | ||||||
| chr1:183412421
|
C | T | 1 | a0001c0001t0030g0169 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.85+5762G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412421 | ||||||
| chr1:183412463
|
C | T | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+5720G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412463 | ||||||
| chr1:183412478
|
C | A | 158 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.85+5705G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412478 | ||||||
| chr1:183412509
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+5674G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412509 | ||||||
| chr1:183412623
|
T | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+5560A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412623 | ||||||
| chr1:183412660
|
G | A | 26 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+5523C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412660 | ||||||
| chr1:183412712
|
A | G | 7 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(4): Show | 7 | HG03516.hp1 NA18950.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+5471T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412712 | ||||||
| chr1:183412817
|
G | A | 1 | a0001c0001t0066g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85+5366C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412817 | ||||||
| chr1:183412846
|
C | T | 2 | a0001c0001t0011g0192a0001c0001t0077g0193 | 2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.85+5337G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412846 | ||||||
| chr1:183412924
|
A | C | 1 | a0001c0001t0011g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.85+5259T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183412924 | ||||||
| chr1:183413058
|
C | T | 5 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(2): Show | 5 | NA18950.hp1 NA18956.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+5125G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413058 | ||||||
| chr1:183413368
|
A | G | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+4815T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413368 | ||||||
| chr1:183413369
|
T | TG | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+4813dupC | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413369 | ||||||
| chr1:183413525
|
C | T | 3 | a0001c0001t0010g0009a0001c0001t0010g0011a0001c0001t0072g0010 | 3 | HG01952.hp2 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.85+4658G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413525 | ||||||
| chr1:183413554
|
T | C | 1 | a0001c0001t0002g0001 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.85+4629A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413554 | ||||||
| chr1:183413602
|
C | CT | 9 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0009g0144others(6): Show | 9 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+4580dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413602 | ||||||
| chr1:183413602
|
C | CTTT | 7 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+4578_85+4580dup others(3): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413602 | ||||||
| chr1:183413602
|
CT | C | 151 | a0001c0001t0001g0045a0001c0001t0001g0227a0001c0001t0001g0228others(148): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.85+4580delA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413602 | ||||||
| chr1:183413602
|
CTT | C | 56 | a0001c0001t0001g0101a0001c0001t0001g0124a0001c0001t0001g0125others(53): Show | 56 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.85+4579_85+4580del others(2): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413602 | ||||||
| chr1:183413604
|
T | TTTTTTTT others(1372): Show |
2 | a0001c0001t0006g0007a0001c0001t0069g0008 | 2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.85+4578_85+4579ins others(1379): Show |
NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413604 | ||||||
| chr1:183413763
|
C | G | 1 | a0001c0001t0001g0035 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.85+4420G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413763 | ||||||
| chr1:183413770
|
C | T | 4 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016others(1): Show | 4 | HG01069.hp1 HG02258.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+4413G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413770 | ||||||
| chr1:183413773
|
A | AT | 26 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0127others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+4409dupA | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413773 | ||||||
| chr1:183413854
|
G | T | 157 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.85+4329C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413854 | ||||||
| chr1:183413895
|
C | T | 1 | a0001c0001t0020g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+4288G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183413895 | ||||||
| chr1:183414107
|
A | T | 1 | a0001c0001t0082g0034 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.85+4076T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414107 | ||||||
| chr1:183414140
|
G | T | 1 | a0001c0001t0026g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+4043C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414140 | ||||||
| chr1:183414207
|
A | G | 1 | a0001c0001t0073g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.85+3976T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414207 | ||||||
| chr1:183414224
|
T | C | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG01069.hp1 HG03516.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+3959A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414224 | ||||||
| chr1:183414227
|
T | A | 168 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.85+3956A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414227 | ||||||
| chr1:183414354
|
C | A | 1 | a0001c0001t0005g0077 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+3829G>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414354 | ||||||
| chr1:183414411
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.85+3772G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414411 | ||||||
| chr1:183414508
|
T | C | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.85+3675A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414508 | ||||||
| chr1:183414723
|
C | G | 2 | a0001c0001t0066g0116a0001c0001t0093g0115 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+3460G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414723 | ||||||
| chr1:183414981
|
GA | G | 35 | a0001c0001t0001g0101a0001c0001t0002g0086a0001c0001t0004g0006others(32): Show | 35 | HG00423.hp1 HG00423.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.85+3201delT | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414981 | ||||||
| chr1:183414990
|
T | A | 3 | a0001c0001t0009g0078a0001c0001t0012g0080a0001c0001t0038g0079 | 3 | NA18975.hp1 NA19005.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.85+3193A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183414990 | ||||||
| chr1:183415190
|
A | C | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+2993T>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415190 | ||||||
| chr1:183415260
|
G | A | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.85+2923C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415260 | ||||||
| chr1:183415335
|
A | G | 1 | a0001c0001t0009g0084 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+2848T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415335 | ||||||
| chr1:183415661
|
G | A | 168 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.85+2522C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415661 | ||||||
| chr1:183415737
|
G | T | 1 | a0001c0001t0021g0083 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.85+2446C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415737 | ||||||
| chr1:183415750
|
A | G | 1 | a0001c0001t0035g0031 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.85+2433T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415750 | ||||||
| chr1:183415828
|
G | C | 15 | a0001c0001t0004g0178a0001c0001t0007g0183a0001c0001t0016g0175others(12): Show | 15 | HG01109.hp2 HG02074.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.85+2355C>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415828 | ||||||
| chr1:183415831
|
T | A | 1 | a0001c0001t0032g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.85+2352A>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183415831 | ||||||
| chr1:183416187
|
A | G | 5 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0010g0026others(2): Show | 5 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1996T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183416187 | ||||||
| chr1:183416318
|
A | T | 1 | a0001c0001t0071g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.85+1865T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183416318 | ||||||
| chr1:183416694
|
C | T | 2 | a0001c0001t0002g0082a0001c0001t0033g0246 | 2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+1489G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183416694 | ||||||
| chr1:183416745
|
T | C | 1 | a0001c0001t0051g0081 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.85+1438A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183416745 | ||||||
| chr1:183417177
|
C | T | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+1006G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417177 | ||||||
| chr1:183417279
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(1): Show | 4 | NA18953.hp2 NA18977.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+904A>G | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417279 | ||||||
| chr1:183417402
|
A | G | 62 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(59): Show | 62 | HG00140.hp2 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.85+781T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417402 | ||||||
| chr1:183417499
|
G | T | 1 | a0001c0001t0030g0017 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.85+684C>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417499 | ||||||
| chr1:183417604
|
C | G | 8 | a0001c0001t0007g0019a0001c0001t0007g0020a0001c0001t0007g0021others(5): Show | 8 | HG01069.hp1 HG03516.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.85+579G>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417604 | ||||||
| chr1:183417653
|
C | T | 3 | a0001c0001t0011g0015a0001c0001t0025g0014a0001c0001t0025g0016 | 3 | HG02258.hp2 HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.85+530G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417653 | ||||||
| chr1:183417693
|
C | T | 193 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0045others(190): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.85+490G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417693 | ||||||
| chr1:183417829
|
C | T | 5 | a0001c0001t0002g0013a0001c0001t0010g0009a0001c0001t0010g0011others(2): Show | 5 | HG01952.hp2 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+354G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417829 | ||||||
| chr1:183417963
|
C | T | 4 | a0001c0001t0004g0006a0001c0001t0005g0005a0001c0001t0006g0007others(1): Show | 4 | HG00423.hp2 HG02129.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+220G>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417963 | ||||||
| chr1:183417967
|
G | A | 1 | a0001c0001t0033g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+216C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183417967 | ||||||
| chr1:183418037
|
G | A | 11 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0016g0253others(8): Show | 11 | HG01099.hp1 HG02109.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+146C>T | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183418037 | ||||||
| chr1:183418092
|
A | T | 1 | a0001c0001t0026g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85+91T>A | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183418092 | ||||||
| chr1:183418161
|
A | G | 2 | a0001c0001t0017g0002a0001c0001t0092g0003 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.85+22T>C | NMNAT2 | ENSG00000157064.11 | transcript | ENST00000287713.7 | protein_coding | 1/10 | chr1 | 183418161 |