| geneid | 349565 |
|---|---|
| ensemblid | ENSG00000163864.18 |
| hgncid | 20989 |
| symbol | NMNAT3 |
| name | nicotinamide nucleotide adenylyltransferase 3 |
| refseq_nuc | NM_001401600.1 |
| refseq_prot | NP_001388529.1 |
| ensembl_nuc | ENST00000704800.1 |
| ensembl_prot | ENSP00000516041.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 139560191 |
| end | 139677972 |
| strand | - |
| ver | v1.2 |
| region | chr3:139560191-139677972 |
| region5000 | chr3:139555191-139682972 |
| regionname0 | NMNAT3_chr3_139560191_139677972 |
| regionname5000 | NMNAT3_chr3_139555191_139682972 |
| 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 | 252 | 319 | 84 | 64 | 120 | 16 | 33 | 90 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0002 | 0/0 | 252 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0003 | 0/0 | 252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0004 | 0/0 | 252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| 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 | 759 | 301 | 71 | 60 | 120 | 16 | 32 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0002 | 0/0 | 759 | 9 | 7 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0003 | 0/0 | 759 | 6 | 4 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0004 | 0/0 | 759 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0005 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0006 | 0/0 | 759 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0007 | 0/0 | 759 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| c0008 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| 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 | 1265 | 216 | 49 | 38 | 94 | 11 | 24 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0002 | 0/1 | 1265 | 89 | 32 | 20 | 21 | 5 | 10 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0003 | 0/0 | 1265 | 5 | 2 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0004 | 0/0 | 1265 | 3 | 0 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0005 | 0/0 | 1265 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0006 | 0/0 | 1265 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0007 | 1/0 | 1265 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0008 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0009 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0010 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0011 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| t0012 | 0/0 | 1265 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| 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 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| 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 | 759 | 301 | 71 | 60 | 120 | 16 | 32 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0002 | 0/0 | 759 | 9 | 7 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0003 | 0/0 | 759 | 6 | 4 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0004 | 0/0 | 759 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0007 | 0/0 | 759 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0002c0006 | 0/0 | 759 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0003c0005 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0004c0008 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2023 | 204 | 41 | 36 | 94 | 11 | 22 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0002 | 0/1 | 2023 | 80 | 25 | 18 | 21 | 5 | 10 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0003 | 0/0 | 2023 | 5 | 2 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0004 | 0/0 | 2023 | 3 | 0 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0005 | 0/0 | 2023 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0006 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0007 | 1/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0008 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0009 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0010 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0011 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0001t0012 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0002t0001 | 0/0 | 2023 | 5 | 4 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0002t0002 | 0/0 | 2023 | 4 | 3 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0003t0001 | 0/0 | 2023 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0003t0002 | 0/0 | 2023 | 4 | 3 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0004t0001 | 0/0 | 2023 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0001c0007t0001 | 0/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0002c0006t0001 | 0/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0003c0005t0002 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| a0004c0008t0001 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | copy fasta | chr3 | 139555191 | 139682972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0034 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0007g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0012g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0007t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0002c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0003c0005t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0004c0008t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0052 | EUR | GBR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0193 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0032 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0090 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0097 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0061 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0125 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0120 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02965 | hp1 | a0003 | c0005 | t0002 | g0030 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03492 | hp2 | a0001 | c0007 | t0001 | g0255 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03942 | hp2 | a0002 | c0006 | t0001 | g0254 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0271 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18980 | hp2 | a0001 | c0001 | t0012 | g0262 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0299 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19030 | hp2 | a0004 | c0008 | t0001 | g0160 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19062 | hp1 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | GIH | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0091 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0088 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0034 | REF | REF | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0017 | REF | REF | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139573651
|
G | A | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.323C>T | p.Pro108Leu | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 768/2023 | 323/759 | 108/252 | chr3 | 139573651 | ||
| chr3:139573652
|
G | A | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.322C>T | p.Pro108Ser | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 767/2023 | 322/759 | 108/252 | chr3 | 139573652 | ||
| chr3:139573668
|
G | C | 1 | a0002 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.306C>G | p.Ser102Arg | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 751/2023 | 306/759 | 102/252 | chr3 | 139573668 | ||
| chr3:139627708
|
G | C | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.17C>G | p.Pro6Arg | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/7 | 462/2023 | 17/759 | 6/252 | chr3 | 139627708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139561094
|
C | T | 1 | a0001c0003 | 6 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(3): Show |
synonymous_variant | LOW | c.675G>A | p.Thr225Thr | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 1120/2023 | 675/759 | 225/252 | chr3 | 139561094 | ||
| chr3:139561109
|
G | A | 1 | a0001c0004 | 2 | HG02896.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.660C>T | p.Pro220Pro | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 1105/2023 | 660/759 | 220/252 | chr3 | 139561109 | ||
| chr3:139578991
|
G | A | 1 | a0001c0002 | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
synonymous_variant | LOW | c.174C>T | p.Leu58Leu | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/7 | 619/2023 | 174/759 | 58/252 | chr3 | 139578991 | ||
| chr3:139579015
|
G | A | 1 | a0001c0007 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.150C>T | p.Asn50Asn | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/7 | 595/2023 | 150/759 | 50/252 | chr3 | 139579015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139560279
|
C | T | 1 | a0001c0001t0009 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 731 | chr3 | 139560279 | |||||
| chr3:139560350
|
T | C | 1 | a0001c0001t0010 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 660 | chr3 | 139560350 | |||||
| chr3:139560431
|
A | G | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*579T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 579 | chr3 | 139560431 | |||||
| chr3:139560690
|
C | T | 1 | a0001c0001t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 320 | chr3 | 139560690 | |||||
| chr3:139560847
|
G | A | 1 | a0001c0001t0011 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 163 | chr3 | 139560847 | |||||
| chr3:139560860
|
G | A | 1 | a0001c0001t0012 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 150 | chr3 | 139560860 | |||||
| chr3:139560874
|
C | T | 1 | a0001c0001t0006 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*136G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 136 | chr3 | 139560874 | |||||
| chr3:139677892
|
T | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 231 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
5_prime_UTR_variant | MODIFIER | c.-365A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | 50168 | chr3 | 139677892 | |||||
| chr3:139677916
|
G | A | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(11): Show | 228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-389C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | chr3 | 139677916 | ||||||
| chr3:139677958
|
G | T | 1 | a0001c0001t0005 | 2 | HG03453.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-431C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | 50234 | chr3 | 139677958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139561486
|
G | GA | 272 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.377-95dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561486 | ||||||
| chr3:139561580
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.377-188A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561580 | ||||||
| chr3:139561617
|
A | G | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-225T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561617 | ||||||
| chr3:139561634
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.377-242G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561634 | ||||||
| chr3:139561794
|
C | A | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-402G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561794 | ||||||
| chr3:139561843
|
A | G | 85 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0133others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-451T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561843 | ||||||
| chr3:139561990
|
GT | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0132a0001c0001t0001g0142others(27): Show | 31 | HG01192.hp1 HG02027.hp2 HG02165.hp2 others(28): Show |
intron_variant | MODIFIER | c.377-599delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561990 | ||||||
| chr3:139562090
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-698G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562090 | ||||||
| chr3:139562127
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0278 | 2 | NA18978.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.377-735T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562127 | ||||||
| chr3:139562142
|
A | ATTG | 85 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0133others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-753_377-751dup others(3): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562142 | ||||||
| chr3:139562311
|
C | T | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.377-919G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562311 | ||||||
| chr3:139562349
|
C | G | 85 | a0001c0001t0001g0116a0001c0001t0001g0128a0001c0001t0001g0133others(82): Show | 85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-957G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562349 | ||||||
| chr3:139562370
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-978C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562370 | ||||||
| chr3:139562750
|
A | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.377-1358T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562750 | ||||||
| chr3:139562994
|
C | T | 9 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0168others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-1602G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562994 | ||||||
| chr3:139563026
|
T | C | 4 | a0001c0001t0001g0295a0001c0001t0002g0019a0001c0001t0002g0076others(1): Show | 4 | HG02027.hp2 NA18953.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1634A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563026 | ||||||
| chr3:139563060
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.377-1668A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563060 | ||||||
| chr3:139563074
|
T | C | 1 | a0001c0001t0004g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.377-1682A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563074 | ||||||
| chr3:139563344
|
C | A | 79 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-1952G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563344 | ||||||
| chr3:139563538
|
C | T | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.377-2146G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563538 | ||||||
| chr3:139563544
|
A | G | 1 | a0001c0001t0002g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.377-2152T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563544 | ||||||
| chr3:139563618
|
T | C | 4 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(1): Show | 4 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2226A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563618 | ||||||
| chr3:139563709
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.377-2317G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563709 | ||||||
| chr3:139563728
|
G | C | 81 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.377-2336C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563728 | ||||||
| chr3:139563733
|
A | G | 10 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0168others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-2341T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563733 | ||||||
| chr3:139563739
|
G | A | 79 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-2347C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563739 | ||||||
| chr3:139563856
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0001g0231a0001c0001t0012g0262 | 3 | NA18962.hp2 NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.377-2464C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563856 | ||||||
| chr3:139563861
|
C | A | 80 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.377-2469G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563861 | ||||||
| chr3:139563865
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-2473A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563865 | ||||||
| chr3:139563966
|
A | G | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.377-2574T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563966 | ||||||
| chr3:139564147
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.377-2755T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564147 | ||||||
| chr3:139564224
|
C | A | 2 | a0001c0001t0002g0093a0001c0001t0006g0048 | 2 | HG01169.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.377-2832G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564224 | ||||||
| chr3:139564245
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-2853G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564245 | ||||||
| chr3:139564266
|
G | GT | 15 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-2875dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564266 | ||||||
| chr3:139564372
|
T | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-2980A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564372 | ||||||
| chr3:139564391
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0141 | 2 | NA18993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.377-2999G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564391 | ||||||
| chr3:139564552
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-3160G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564552 | ||||||
| chr3:139564558
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.377-3166G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564558 | ||||||
| chr3:139564562
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-3170G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564562 | ||||||
| chr3:139564620
|
A | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 184 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.377-3228T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564620 | ||||||
| chr3:139564915
|
CAAT | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0231a0001c0001t0001g0240others(3): Show | 6 | NA18962.hp2 NA18972.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-3526_377-3524d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564915 | ||||||
| chr3:139565005
|
A | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-3613T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565005 | ||||||
| chr3:139565131
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-3739C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565131 | ||||||
| chr3:139565162
|
A | G | 15 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.377-3770T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565162 | ||||||
| chr3:139565192
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-3800A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565192 | ||||||
| chr3:139565428
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 176 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.377-4036G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565428 | ||||||
| chr3:139565489
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.377-4097A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565489 | ||||||
| chr3:139565514
|
T | G | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-4122A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565514 | ||||||
| chr3:139565515
|
C | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-4123G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565515 | ||||||
| chr3:139565547
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.377-4155C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565547 | ||||||
| chr3:139565574
|
C | T | 20 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.377-4182G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565574 | ||||||
| chr3:139565608
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0002g0025 | 2 | HG03516.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.377-4216G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565608 | ||||||
| chr3:139565654
|
T | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(74): Show | 80 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-4262A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565654 | ||||||
| chr3:139565716
|
A | T | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.377-4324T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565716 | ||||||
| chr3:139565894
|
G | A | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.377-4502C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565894 | ||||||
| chr3:139566046
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.377-4654A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566046 | ||||||
| chr3:139566047
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.377-4655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566047 | ||||||
| chr3:139566048
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-4656C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566048 | ||||||
| chr3:139566170
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-4778C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566170 | ||||||
| chr3:139566180
|
A | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(71): Show | 75 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.377-4788T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566180 | ||||||
| chr3:139566182
|
A | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-4790T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566182 | ||||||
| chr3:139566309
|
A | G | 271 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(268): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.377-4917T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566309 | ||||||
| chr3:139566339
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0315 | 2 | HG00423.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.377-4947A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566339 | ||||||
| chr3:139566344
|
T | A | 156 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 160 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.377-4952A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566344 | ||||||
| chr3:139566557
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5165T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566557 | ||||||
| chr3:139566644
|
C | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 179 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.377-5252G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566644 | ||||||
| chr3:139566718
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(74): Show | 80 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-5326G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566718 | ||||||
| chr3:139566734
|
G | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 179 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.377-5342C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566734 | ||||||
| chr3:139566844
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-5452C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566844 | ||||||
| chr3:139566889
|
A | G | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.377-5497T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566889 | ||||||
| chr3:139566922
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.377-5530T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566922 | ||||||
| chr3:139566928
|
C | T | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5536G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566928 | ||||||
| chr3:139567089
|
A | C | 124 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(121): Show | 125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.377-5697T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567089 | ||||||
| chr3:139567250
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377-5858T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567250 | ||||||
| chr3:139567267
|
G | A | 79 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-5875C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567267 | ||||||
| chr3:139567298
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5906A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567298 | ||||||
| chr3:139567336
|
C | G | 1 | a0001c0001t0001g0296 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.377-5944G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567336 | ||||||
| chr3:139567368
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5976A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567368 | ||||||
| chr3:139567438
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.377-6046G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567438 | ||||||
| chr3:139567468
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-6076G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567468 | ||||||
| chr3:139567654
|
C | A | 2 | a0001c0001t0001g0140a0001c0001t0001g0227 | 2 | NA18970.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.376+5944G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567654 | ||||||
| chr3:139567655
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.376+5943T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567655 | ||||||
| chr3:139567770
|
G | A | 19 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.376+5828C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567770 | ||||||
| chr3:139567851
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.376+5747G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567851 | ||||||
| chr3:139567866
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.376+5732T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567866 | ||||||
| chr3:139568117
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376+5481C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568117 | ||||||
| chr3:139568334
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+5264G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568334 | ||||||
| chr3:139568338
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+5260A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568338 | ||||||
| chr3:139568449
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.376+5149C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568449 | ||||||
| chr3:139568465
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.376+5133C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568465 | ||||||
| chr3:139568530
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0174a0001c0001t0001g0180others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+5068A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568530 | ||||||
| chr3:139568552
|
C | A | 176 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 180 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.376+5046G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568552 | ||||||
| chr3:139568553
|
A | G | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.376+5045T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568553 | ||||||
| chr3:139568595
|
A | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.376+5003T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568595 | ||||||
| chr3:139568630
|
G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0277 | 2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.376+4968C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568630 | ||||||
| chr3:139568642
|
C | T | 1 | a0001c0001t0002g0094 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.376+4956G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568642 | ||||||
| chr3:139568647
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376+4951G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568647 | ||||||
| chr3:139568766
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.376+4832C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568766 | ||||||
| chr3:139568782
|
T | C | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376+4816A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568782 | ||||||
| chr3:139569011
|
T | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.376+4587A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569011 | ||||||
| chr3:139569115
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0257 | 2 | HG00323.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.376+4483A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569115 | ||||||
| chr3:139569179
|
GTT | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+4417_376+4418d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569179 | ||||||
| chr3:139569201
|
C | G | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+4397G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569201 | ||||||
| chr3:139569272
|
C | CTGA | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.376+4323_376+4325d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569272 | ||||||
| chr3:139569490
|
C | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0290 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.376+4108G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569490 | ||||||
| chr3:139569530
|
C | G | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+4068G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569530 | ||||||
| chr3:139569702
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+3896G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569702 | ||||||
| chr3:139569722
|
T | A | 1 | a0001c0001t0002g0092 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.376+3876A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569722 | ||||||
| chr3:139569749
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.376+3849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569749 | ||||||
| chr3:139569830
|
C | T | 4 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(1): Show | 4 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+3768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569830 | ||||||
| chr3:139569945
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.376+3653C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569945 | ||||||
| chr3:139569962
|
C | T | 173 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(170): Show | 177 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.376+3636G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569962 | ||||||
| chr3:139569997
|
G | T | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0179others(6): Show | 9 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+3601C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569997 | ||||||
| chr3:139570130
|
C | T | 5 | a0001c0001t0001g0301a0001c0002t0001g0122a0001c0002t0001g0124others(2): Show | 5 | HG01175.hp1 HG02273.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+3468G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570130 | ||||||
| chr3:139570142
|
T | C | 10 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0168others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.376+3456A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570142 | ||||||
| chr3:139570145
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376+3453C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570145 | ||||||
| chr3:139570319
|
G | T | 95 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.376+3279C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570319 | ||||||
| chr3:139570458
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.376+3140A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570458 | ||||||
| chr3:139570459
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0002g0020others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+3139G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570459 | ||||||
| chr3:139570571
|
C | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.376+3027G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570571 | ||||||
| chr3:139570607
|
C | A | 94 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.376+2991G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570607 | ||||||
| chr3:139570692
|
G | A | 77 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(74): Show | 77 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.376+2906C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570692 | ||||||
| chr3:139570699
|
T | C | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0179others(6): Show | 9 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+2899A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570699 | ||||||
| chr3:139570748
|
C | T | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376+2850G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570748 | ||||||
| chr3:139570776
|
C | T | 94 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.376+2822G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570776 | ||||||
| chr3:139570956
|
G | T | 95 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(92): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.376+2642C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570956 | ||||||
| chr3:139571010
|
C | T | 20 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.376+2588G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571010 | ||||||
| chr3:139571011
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+2587C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571011 | ||||||
| chr3:139571036
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.376+2562T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571036 | ||||||
| chr3:139571040
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.376+2558G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571040 | ||||||
| chr3:139571049
|
C | T | 1 | a0001c0003t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.376+2549G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571049 | ||||||
| chr3:139571143
|
C | T | 20 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.376+2455G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571143 | ||||||
| chr3:139571178
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2420C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571178 | ||||||
| chr3:139571201
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2397G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571201 | ||||||
| chr3:139571202
|
G | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.376+2396C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571202 | ||||||
| chr3:139571240
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2358G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571240 | ||||||
| chr3:139571324
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2274G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571324 | ||||||
| chr3:139571335
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376+2263G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571335 | ||||||
| chr3:139571336
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376+2262C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571336 | ||||||
| chr3:139571388
|
T | C | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376+2210A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571388 | ||||||
| chr3:139571426
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376+2172C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571426 | ||||||
| chr3:139571476
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.376+2122G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571476 | ||||||
| chr3:139571477
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2121C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571477 | ||||||
| chr3:139571513
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+2085G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571513 | ||||||
| chr3:139571602
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.376+1996T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571602 | ||||||
| chr3:139571627
|
C | T | 81 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+1971G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571627 | ||||||
| chr3:139571683
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.376+1915C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571683 | ||||||
| chr3:139571746
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0286others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+1852G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571746 | ||||||
| chr3:139571776
|
C | T | 1 | a0001c0001t0001g0309 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.376+1822G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571776 | ||||||
| chr3:139571938
|
C | A | 1 | a0001c0001t0002g0038 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.376+1660G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571938 | ||||||
| chr3:139571955
|
C | T | 15 | a0001c0001t0001g0106a0001c0001t0001g0116a0001c0001t0001g0121others(12): Show | 15 | HG01109.hp1 HG01175.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.376+1643G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571955 | ||||||
| chr3:139571969
|
A | G | 81 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+1629T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571969 | ||||||
| chr3:139572085
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.376+1513G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572085 | ||||||
| chr3:139572102
|
C | A | 1 | a0001c0001t0006g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.376+1496G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572102 | ||||||
| chr3:139572129
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+1469C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572129 | ||||||
| chr3:139572378
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.376+1220T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572378 | ||||||
| chr3:139572492
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0020 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.376+1106G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572492 | ||||||
| chr3:139572575
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+1023C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572575 | ||||||
| chr3:139572768
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.376+830G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572768 | ||||||
| chr3:139572831
|
A | G | 81 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+767T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572831 | ||||||
| chr3:139572907
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.376+691G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572907 | ||||||
| chr3:139572964
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.376+634G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572964 | ||||||
| chr3:139572973
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+625C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572973 | ||||||
| chr3:139573045
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0002g0020others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+553G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573045 | ||||||
| chr3:139573180
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0002g0083 | 2 | NA18980.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.376+418G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573180 | ||||||
| chr3:139573238
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.376+360C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573238 | ||||||
| chr3:139573254
|
A | G | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+344T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573254 | ||||||
| chr3:139573493
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.376+105C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573493 | ||||||
| chr3:139573541
|
G | T | 1 | a0001c0001t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+57C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573541 | ||||||
| chr3:139573953
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.294-273G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139573953 | ||||||
| chr3:139573972
|
CA | C | 12 | a0001c0001t0001g0119a0001c0001t0001g0259a0001c0002t0001g0122others(9): Show | 12 | HG01123.hp1 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.294-293delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139573972 | ||||||
| chr3:139574246
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.294-566G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574246 | ||||||
| chr3:139574266
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.294-586G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574266 | ||||||
| chr3:139574311
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.294-631G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574311 | ||||||
| chr3:139574500
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.294-820A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574500 | ||||||
| chr3:139574892
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.294-1212T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574892 | ||||||
| chr3:139575101
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.294-1421A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575101 | ||||||
| chr3:139575268
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.294-1588C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575268 | ||||||
| chr3:139575363
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294-1683G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575363 | ||||||
| chr3:139575430
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.294-1750G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575430 | ||||||
| chr3:139575641
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.294-1961A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575641 | ||||||
| chr3:139575674
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.294-1994G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575674 | ||||||
| chr3:139576137
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294-2457C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576137 | ||||||
| chr3:139576220
|
A | AT | 6 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0001g0304others(3): Show | 6 | NA18612.hp1 NA18946.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-2541dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576220 | ||||||
| chr3:139576265
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.294-2585G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576265 | ||||||
| chr3:139576296
|
G | A | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(233): Show | 240 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.293+2576C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576296 | ||||||
| chr3:139576304
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.293+2568T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576304 | ||||||
| chr3:139576512
|
TATTAAGT others(1): Show |
T | 69 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(66): Show | 70 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(67): Show |
intron_variant | MODIFIER | c.293+2352_293+2359d others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576512 | ||||||
| chr3:139576529
|
A | G | 6 | a0001c0001t0001g0213a0001c0001t0001g0244a0001c0001t0001g0304others(3): Show | 6 | NA18612.hp1 NA18946.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+2343T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576529 | ||||||
| chr3:139576653
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293+2219G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576653 | ||||||
| chr3:139576712
|
C | A | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+2160G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576712 | ||||||
| chr3:139576750
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.293+2122T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576750 | ||||||
| chr3:139576777
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293+2095G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576777 | ||||||
| chr3:139576885
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.293+1987C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576885 | ||||||
| chr3:139577099
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.293+1773T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577099 | ||||||
| chr3:139577110
|
T | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+1762A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577110 | ||||||
| chr3:139577124
|
T | TC | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+1747dupG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577124 | ||||||
| chr3:139577125
|
C | CA | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(91): Show | 97 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.293+1746dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577125 | ||||||
| chr3:139577371
|
C | T | 5 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+1501G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577371 | ||||||
| chr3:139577381
|
G | C | 2 | a0001c0001t0001g0223a0001c0001t0002g0057 | 2 | NA18959.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.293+1491C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577381 | ||||||
| chr3:139577849
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293+1023T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577849 | ||||||
| chr3:139577870
|
A | T | 79 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.293+1002T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577870 | ||||||
| chr3:139577936
|
T | C | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.293+936A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577936 | ||||||
| chr3:139578001
|
T | TG | 9 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0168others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.293+870dupC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578001 | ||||||
| chr3:139578389
|
C | A | 5 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+483G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578389 | ||||||
| chr3:139578722
|
CT | C | 15 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.293+149delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578722 | ||||||
| chr3:139578800
|
C | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0218 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.293+72G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578800 | ||||||
| chr3:139578813
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+59T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578813 | ||||||
| chr3:139578838
|
C | T | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.293+34G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578838 | ||||||
| chr3:139578851
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293+21G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578851 | ||||||
| chr3:139579146
|
G | T | 5 | a0001c0001t0001g0215a0001c0001t0001g0270a0001c0001t0001g0276others(2): Show | 5 | NA18941.hp1 NA18978.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-91C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579146 | ||||||
| chr3:139579269
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0002g0020 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-214G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579269 | ||||||
| chr3:139579357
|
C | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.110-302G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579357 | ||||||
| chr3:139579519
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-464C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579519 | ||||||
| chr3:139579704
|
G | T | 12 | a0001c0001t0001g0194a0001c0001t0002g0039a0001c0001t0002g0058others(9): Show | 12 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-649C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579704 | ||||||
| chr3:139579725
|
T | G | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.110-670A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579725 | ||||||
| chr3:139579804
|
T | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(69): Show | 73 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.110-749A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579804 | ||||||
| chr3:139579836
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.110-781T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579836 | ||||||
| chr3:139579908
|
T | G | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-853A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579908 | ||||||
| chr3:139580036
|
G | A | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-981C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580036 | ||||||
| chr3:139580236
|
T | TCTCAGCT others(41): Show |
14 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0194others(11): Show | 14 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-1182_110-1181i others(50): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580236 | ||||||
| chr3:139580284
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.110-1229C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580284 | ||||||
| chr3:139580386
|
G | T | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-1331C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580386 | ||||||
| chr3:139580425
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-1370T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580425 | ||||||
| chr3:139580814
|
C | CT | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(78): Show | 84 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.110-1760dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580814 | ||||||
| chr3:139580958
|
C | G | 1 | a0001c0001t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.110-1903G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580958 | ||||||
| chr3:139581078
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-2023T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581078 | ||||||
| chr3:139581172
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-2117G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581172 | ||||||
| chr3:139581303
|
A | ATAT | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.110-2251_110-2249d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581303 | ||||||
| chr3:139581369
|
C | CT | 17 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(14): Show | 18 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.110-2315dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | ||||||
| chr3:139581369
|
CT | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0106a0001c0001t0001g0156others(43): Show | 47 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-2315delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | ||||||
| chr3:139581369
|
CTT | C | 7 | a0001c0002t0001g0122a0001c0002t0001g0125a0001c0002t0001g0195others(4): Show | 7 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-2316_110-2315d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | ||||||
| chr3:139581378
|
T | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-2323A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581378 | ||||||
| chr3:139581647
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-2592A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581647 | ||||||
| chr3:139581717
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110-2662A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581717 | ||||||
| chr3:139581926
|
GGCTCATG others(440): Show |
G | 1 | a0001c0001t0004g0096 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.110-3318_110-2872d others(2): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581926 | ||||||
| chr3:139581939
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-2884T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581939 | ||||||
| chr3:139582085
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3030G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582085 | ||||||
| chr3:139582093
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-3038C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582093 | ||||||
| chr3:139582171
|
A | G | 17 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-3116T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582171 | ||||||
| chr3:139582190
|
C | CA | 25 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0001t0001g0107others(22): Show | 25 | HG01074.hp2 HG01175.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.110-3136dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | ||||||
| chr3:139582190
|
CA | C | 18 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0117others(15): Show | 18 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-3136delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | ||||||
| chr3:139582190
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.110-3151_110-3136d others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | ||||||
| chr3:139582206
|
A | G | 13 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(10): Show | 13 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-3151T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582206 | ||||||
| chr3:139582214
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.110-3159T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582214 | ||||||
| chr3:139582215
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0215 | 2 | HG04199.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.110-3160C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582215 | ||||||
| chr3:139582216
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-3161T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582216 | ||||||
| chr3:139582336
|
T | G | 80 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-3281A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582336 | ||||||
| chr3:139582639
|
C | CA | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.110-3585dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | ||||||
| chr3:139582639
|
C | CAA | 21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0105others(18): Show | 21 | HG00423.hp1 HG00621.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-3586_110-3585d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | ||||||
| chr3:139582639
|
CA | C | 14 | a0001c0001t0001g0118a0001c0001t0001g0126a0001c0001t0001g0289others(11): Show | 14 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-3585delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | ||||||
| chr3:139582639
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-3595_110-3585d others(13): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | ||||||
| chr3:139582907
|
A | T | 13 | a0001c0001t0001g0289a0001c0001t0001g0296a0001c0001t0002g0010others(10): Show | 13 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.110-3852T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582907 | ||||||
| chr3:139582909
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-3854A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582909 | ||||||
| chr3:139582939
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.110-3884G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582939 | ||||||
| chr3:139582956
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110-3901A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582956 | ||||||
| chr3:139583034
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-3979G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583034 | ||||||
| chr3:139583315
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-4260T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583315 | ||||||
| chr3:139583415
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.110-4360A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583415 | ||||||
| chr3:139583495
|
T | TTCTGAAG others(138): Show |
79 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.110-4585_110-4441d others(147): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583495 | ||||||
| chr3:139583495
|
TTCTGAAG others(138): Show |
T | 10 | a0001c0001t0001g0281a0001c0002t0001g0122a0001c0002t0001g0124others(7): Show | 10 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-4585_110-4441d others(2): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583495 | ||||||
| chr3:139583634
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110-4579G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583634 | ||||||
| chr3:139584083
|
CA | C | 9 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0199others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-5029delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584083 | ||||||
| chr3:139584235
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-5180C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584235 | ||||||
| chr3:139584248
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-5193T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584248 | ||||||
| chr3:139584286
|
C | T | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-5231G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584286 | ||||||
| chr3:139584343
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-5288G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584343 | ||||||
| chr3:139584406
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(277): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.110-5351C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584406 | ||||||
| chr3:139584789
|
A | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-5734T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584789 | ||||||
| chr3:139584902
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-5847C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584902 | ||||||
| chr3:139584914
|
C | T | 1 | a0001c0007t0001g0255 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.110-5859G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584914 | ||||||
| chr3:139585045
|
T | G | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-5990A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585045 | ||||||
| chr3:139585098
|
C | T | 80 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-6043G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585098 | ||||||
| chr3:139585143
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-6088G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585143 | ||||||
| chr3:139585413
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.110-6358G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585413 | ||||||
| chr3:139585531
|
A | G | 1 | a0001c0004t0001g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.110-6476T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585531 | ||||||
| chr3:139585541
|
G | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(75): Show | 81 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.110-6486C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585541 | ||||||
| chr3:139585996
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-6941G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585996 | ||||||
| chr3:139586160
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.110-7105A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586160 | ||||||
| chr3:139586227
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0257 | 2 | HG00323.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.110-7172C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586227 | ||||||
| chr3:139586271
|
C | A | 1 | a0001c0001t0001g0249 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110-7216G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586271 | ||||||
| chr3:139586443
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-7388A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586443 | ||||||
| chr3:139586492
|
T | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-7437A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586492 | ||||||
| chr3:139586662
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.110-7607G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586662 | ||||||
| chr3:139586702
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0141 | 2 | NA18993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.110-7647C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586702 | ||||||
| chr3:139586755
|
G | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-7700C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586755 | ||||||
| chr3:139587054
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-7999C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587054 | ||||||
| chr3:139587266
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-8211C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587266 | ||||||
| chr3:139587322
|
G | A | 10 | a0001c0001t0001g0126a0001c0001t0001g0187a0001c0001t0001g0194others(7): Show | 10 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-8267C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587322 | ||||||
| chr3:139587345
|
T | G | 10 | a0001c0001t0001g0126a0001c0001t0001g0187a0001c0001t0001g0194others(7): Show | 10 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-8290A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587345 | ||||||
| chr3:139587425
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.110-8370G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587425 | ||||||
| chr3:139587442
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-8387G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587442 | ||||||
| chr3:139587470
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.110-8415G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587470 | ||||||
| chr3:139587649
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-8594T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587649 | ||||||
| chr3:139587650
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-8595G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587650 | ||||||
| chr3:139587733
|
A | C | 83 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.110-8678T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587733 | ||||||
| chr3:139587786
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.110-8731C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587786 | ||||||
| chr3:139587986
|
A | G | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 265 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.110-8931T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587986 | ||||||
| chr3:139588058
|
T | G | 1 | a0001c0001t0001g0291 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.110-9003A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588058 | ||||||
| chr3:139588318
|
G | A | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-9263C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588318 | ||||||
| chr3:139588369
|
G | A | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-9314C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588369 | ||||||
| chr3:139588488
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.110-9433A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588488 | ||||||
| chr3:139588533
|
G | T | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-9478C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588533 | ||||||
| chr3:139588619
|
C | G | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-9564G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588619 | ||||||
| chr3:139588633
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9578C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588633 | ||||||
| chr3:139588707
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9652A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588707 | ||||||
| chr3:139588717
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9662G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588717 | ||||||
| chr3:139588744
|
C | T | 2 | a0001c0001t0001g0310a0001c0001t0002g0065 | 2 | NA18957.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.110-9689G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588744 | ||||||
| chr3:139588820
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-9765T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588820 | ||||||
| chr3:139588880
|
G | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-9825C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588880 | ||||||
| chr3:139589275
|
A | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(77): Show | 83 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.110-10220T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589275 | ||||||
| chr3:139589305
|
G | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-10250C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589305 | ||||||
| chr3:139589477
|
T | C | 8 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0058others(5): Show | 8 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-10422A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589477 | ||||||
| chr3:139589571
|
C | A | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110-10516G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589571 | ||||||
| chr3:139589808
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-10753A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589808 | ||||||
| chr3:139589904
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-10849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589904 | ||||||
| chr3:139589991
|
C | T | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-10936G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589991 | ||||||
| chr3:139590036
|
G | A | 2 | a0001c0001t0002g0018a0001c0001t0002g0051 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.110-10981C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590036 | ||||||
| chr3:139590111
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-11056G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590111 | ||||||
| chr3:139590219
|
A | T | 1 | a0001c0001t0001g0303 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.110-11164T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590219 | ||||||
| chr3:139590449
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-11394C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590449 | ||||||
| chr3:139590692
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-11637C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590692 | ||||||
| chr3:139590982
|
G | GGAACAGC others(6): Show |
3 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0201 | 3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11928_110-1192 others(17): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590982 | ||||||
| chr3:139591009
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0201 | 3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11954A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591009 | ||||||
| chr3:139591011
|
A | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0182a0001c0001t0001g0201 | 3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11956T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591011 | ||||||
| chr3:139591019
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.110-11964T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591019 | ||||||
| chr3:139591059
|
G | A | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-12004C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591059 | ||||||
| chr3:139591091
|
G | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12036C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591091 | ||||||
| chr3:139591281
|
G | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12226C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591281 | ||||||
| chr3:139591316
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110-12261G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591316 | ||||||
| chr3:139591320
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-12265C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591320 | ||||||
| chr3:139591387
|
C | T | 1 | a0001c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-12332G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591387 | ||||||
| chr3:139591419
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12364G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591419 | ||||||
| chr3:139591441
|
G | A | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-12386C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591441 | ||||||
| chr3:139591448
|
G | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.110-12393C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591448 | ||||||
| chr3:139591604
|
C | G | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-12549G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591604 | ||||||
| chr3:139591608
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.110-12553C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591608 | ||||||
| chr3:139591627
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0005g0006 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-12572G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591627 | ||||||
| chr3:139591644
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-12589A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591644 | ||||||
| chr3:139591696
|
C | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0127others(58): Show | 64 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.110-12641G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591696 | ||||||
| chr3:139591708
|
G | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0314 | 2 | NA18906.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.110-12653C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591708 | ||||||
| chr3:139591723
|
A | C | 1 | a0001c0001t0001g0314 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.110-12668T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591723 | ||||||
| chr3:139591727
|
C | A | 1 | a0001c0001t0001g0314 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.110-12672G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591727 | ||||||
| chr3:139591741
|
G | C | 8 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0058others(5): Show | 8 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-12686C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591741 | ||||||
| chr3:139591801
|
C | T | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12746G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591801 | ||||||
| chr3:139591826
|
C | A | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12771G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591826 | ||||||
| chr3:139591866
|
G | A | 83 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.110-12811C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591866 | ||||||
| chr3:139591902
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12847T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591902 | ||||||
| chr3:139591903
|
T | G | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12848A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591903 | ||||||
| chr3:139591909
|
C | T | 1 | a0001c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-12854G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591909 | ||||||
| chr3:139591932
|
G | A | 10 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0199others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-12877C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591932 | ||||||
| chr3:139592058
|
T | C | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-13003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592058 | ||||||
| chr3:139592152
|
T | A | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-13097A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592152 | ||||||
| chr3:139592154
|
G | C | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-13099C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592154 | ||||||
| chr3:139592201
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.110-13146C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592201 | ||||||
| chr3:139592248
|
G | C | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-13193C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592248 | ||||||
| chr3:139592290
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-13235C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592290 | ||||||
| chr3:139592363
|
G | T | 1 | a0001c0001t0005g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-13308C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592363 | ||||||
| chr3:139592470
|
T | G | 2 | a0001c0001t0001g0263a0001c0001t0002g0024 | 2 | HG01106.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.110-13415A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592470 | ||||||
| chr3:139592591
|
G | A | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-13536C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592591 | ||||||
| chr3:139592729
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-13674T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592729 | ||||||
| chr3:139592915
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(67): Show | 71 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-13860G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592915 | ||||||
| chr3:139593081
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14026A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593081 | ||||||
| chr3:139593083
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14028A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593083 | ||||||
| chr3:139593112
|
A | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14057T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593112 | ||||||
| chr3:139593402
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0002g0011 | 2 | HG02486.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110-14347G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593402 | ||||||
| chr3:139593448
|
G | T | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-14393C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593448 | ||||||
| chr3:139593457
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-14402C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593457 | ||||||
| chr3:139593531
|
C | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-14476G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593531 | ||||||
| chr3:139593532
|
C | T | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-14477G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593532 | ||||||
| chr3:139593582
|
G | GTAAAATA others(38): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0218 | 2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.110-14572_110-1452 others(49): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593582 | ||||||
| chr3:139593609
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-14554T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593609 | ||||||
| chr3:139593622
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.110-14567G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593622 | ||||||
| chr3:139593655
|
T | G | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-14600A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593655 | ||||||
| chr3:139593763
|
T | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(67): Show | 71 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-14708A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593763 | ||||||
| chr3:139593784
|
C | T | 1 | a0001c0001t0002g0034 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.110-14729G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593784 | ||||||
| chr3:139593800
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-14745T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593800 | ||||||
| chr3:139593843
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.110-14788G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593843 | ||||||
| chr3:139593852
|
G | C | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.110-14797C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593852 | ||||||
| chr3:139594038
|
A | G | 11 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0018others(8): Show | 11 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-14983T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594038 | ||||||
| chr3:139594058
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0051 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.110-15003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594058 | ||||||
| chr3:139594106
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-15051C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594106 | ||||||
| chr3:139594150
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.110-15095T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594150 | ||||||
| chr3:139594175
|
T | A | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-15120A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594175 | ||||||
| chr3:139594333
|
C | T | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-15278G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594333 | ||||||
| chr3:139594364
|
C | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15309G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594364 | ||||||
| chr3:139594366
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15311A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594366 | ||||||
| chr3:139594396
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.110-15341G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594396 | ||||||
| chr3:139594492
|
T | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15437A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594492 | ||||||
| chr3:139594494
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15439T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594494 | ||||||
| chr3:139594537
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-15482C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594537 | ||||||
| chr3:139594570
|
A | T | 3 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0005g0006 | 3 | HG02723.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-15515T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594570 | ||||||
| chr3:139594580
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-15525G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594580 | ||||||
| chr3:139594581
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-15526C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594581 | ||||||
| chr3:139594688
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.110-15633T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594688 | ||||||
| chr3:139594697
|
A | G | 6 | a0001c0001t0001g0219a0001c0001t0001g0225a0001c0001t0001g0250others(3): Show | 6 | HG00423.hp2 NA18941.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-15642T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594697 | ||||||
| chr3:139594726
|
A | C | 21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-15671T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594726 | ||||||
| chr3:139594779
|
T | G | 15 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-15724A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594779 | ||||||
| chr3:139594849
|
G | A | 5 | a0001c0001t0001g0126a0001c0001t0001g0187a0001c0001t0001g0194others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-15794C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594849 | ||||||
| chr3:139594957
|
G | T | 1 | a0001c0001t0002g0076 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.110-15902C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594957 | ||||||
| chr3:139594998
|
A | G | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-15943T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594998 | ||||||
| chr3:139595037
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.110-15982G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595037 | ||||||
| chr3:139595099
|
A | G | 1 | a0001c0001t0006g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.110-16044T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595099 | ||||||
| chr3:139595369
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-16314C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595369 | ||||||
| chr3:139595423
|
G | C | 281 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.110-16368C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595423 | ||||||
| chr3:139595492
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-16437G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595492 | ||||||
| chr3:139595493
|
G | T | 21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-16438C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595493 | ||||||
| chr3:139595585
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.110-16530T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595585 | ||||||
| chr3:139595629
|
C | T | 1 | a0001c0001t0001g0231 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.110-16574G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595629 | ||||||
| chr3:139595663
|
T | G | 5 | a0001c0002t0001g0175a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-16608A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595663 | ||||||
| chr3:139595708
|
G | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16653C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595708 | ||||||
| chr3:139595710
|
A | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16655T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595710 | ||||||
| chr3:139595711
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16656T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595711 | ||||||
| chr3:139595712
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16657T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595712 | ||||||
| chr3:139595714
|
G | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16659C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595714 | ||||||
| chr3:139595715
|
A | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16660T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595715 | ||||||
| chr3:139595717
|
TCCC | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16665_110-1666 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595717 | ||||||
| chr3:139595728
|
TA | T | 73 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(70): Show | 74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16674delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595728 | ||||||
| chr3:139595887
|
G | T | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-16832C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595887 | ||||||
| chr3:139595946
|
C | T | 16 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(13): Show | 17 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.110-16891G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595946 | ||||||
| chr3:139596136
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.110-17081G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596136 | ||||||
| chr3:139596194
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.110-17139A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596194 | ||||||
| chr3:139596204
|
G | A | 1 | a0001c0001t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.110-17149C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596204 | ||||||
| chr3:139596379
|
T | G | 1 | a0001c0001t0001g0301 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.110-17324A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596379 | ||||||
| chr3:139596397
|
A | C | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-17342T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596397 | ||||||
| chr3:139596561
|
T | C | 2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-17506A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596561 | ||||||
| chr3:139596599
|
A | G | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(93): Show | 100 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.110-17544T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596599 | ||||||
| chr3:139596744
|
T | C | 13 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(10): Show | 13 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-17689A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596744 | ||||||
| chr3:139596860
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0002g0052 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.110-17805G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596860 | ||||||
| chr3:139596896
|
A | G | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-17841T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596896 | ||||||
| chr3:139596910
|
A | ATG | 15 | a0001c0001t0001g0128a0001c0001t0001g0144a0001c0001t0001g0158others(12): Show | 15 | HG01123.hp1 HG01516.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-17857_110-1785 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596910 | ||||||
| chr3:139596916
|
G | GTATA | 3 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0004t0001g0120 | 3 | HG01109.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-17865_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110-17871_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTA | 10 | a0001c0001t0001g0137a0001c0001t0001g0161a0001c0001t0001g0198others(7): Show | 10 | HG00733.hp1 HG02145.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTATA | 12 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(9): Show | 12 | HG00642.hp2 HG01106.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTATAT others(1): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0265a0001c0001t0001g0291 | 3 | HG03017.hp1 NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTATAT others(3): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0156a0001c0001t0001g0237 | 3 | HG00280.hp1 HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTATAT others(7): Show |
4 | a0001c0001t0001g0167a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG00735.hp1 HG01515.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0228 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-17862_110-1786 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
G | GTGTGTAT others(7): Show |
2 | a0001c0001t0002g0032a0001c0001t0002g0033 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTA | G | 10 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(7): Show | 10 | HG01069.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-17863_110-1786 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATA | G | 13 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0133others(10): Show | 13 | HG00423.hp1 HG00621.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-17865_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATA | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0296a0001c0004t0001g0147others(1): Show | 4 | HG00735.hp2 HG02965.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17867_110-1786 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(3): Show |
G | 6 | a0001c0001t0001g0131a0001c0001t0001g0171a0001c0001t0001g0184others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-17871_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(5): Show |
G | 7 | a0001c0001t0001g0130a0001c0001t0001g0139a0001c0001t0001g0168others(4): Show | 7 | HG00099.hp2 HG00642.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-17873_110-1786 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(7): Show |
G | 16 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0190others(13): Show | 18 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-17875_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0172others(15): Show | 18 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.110-17877_110-1786 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(11): Show |
G | 48 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0143others(45): Show | 49 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.110-17879_110-1786 others(22): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(13): Show |
G | 14 | a0001c0001t0001g0135a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-17881_110-1786 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(15): Show |
G | 4 | a0001c0001t0001g0166a0001c0001t0001g0246a0001c0001t0001g0301others(1): Show | 4 | HG02273.hp1 HG03486.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17883_110-1786 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(17): Show |
G | 71 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(68): Show | 72 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(69): Show |
intron_variant | MODIFIER | c.110-17885_110-1786 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-17887_110-1786 others(30): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(21): Show |
G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-17889_110-1786 others(32): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(25): Show |
G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-17893_110-1786 others(36): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(29): Show |
G | 4 | a0001c0001t0001g0194a0001c0001t0001g0256a0001c0001t0002g0058others(1): Show | 4 | HG02717.hp1 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17897_110-1786 others(40): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(31): Show |
G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-17899_110-1786 others(42): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596916
|
GTATATAT others(33): Show |
G | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.110-17901_110-1786 others(44): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | ||||||
| chr3:139596918
|
A | G | 26 | a0001c0001t0001g0099a0001c0001t0001g0136a0001c0001t0001g0141others(23): Show | 26 | HG00639.hp2 HG01175.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.110-17863T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596918 | ||||||
| chr3:139596920
|
A | G | 11 | a0001c0001t0001g0138a0001c0001t0001g0277a0001c0002t0001g0122others(8): Show | 11 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-17865T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596920 | ||||||
| chr3:139596922
|
A | G | 16 | a0001c0001t0001g0098a0001c0001t0001g0133a0001c0001t0001g0224others(13): Show | 16 | HG00423.hp1 HG00621.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-17867T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596922 | ||||||
| chr3:139596926
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0002g0072 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.110-17871T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596926 | ||||||
| chr3:139596928
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0257 | 2 | HG00323.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.110-17873T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596928 | ||||||
| chr3:139596930
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0317 | 2 | HG01081.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.110-17875T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596930 | ||||||
| chr3:139596932
|
A | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0190others(13): Show | 18 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-17877T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596932 | ||||||
| chr3:139596934
|
A | G | 17 | a0001c0001t0001g0110a0001c0001t0001g0127a0001c0001t0001g0172others(14): Show | 17 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-17879T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596934 | ||||||
| chr3:139596936
|
A | G | 48 | a0001c0001t0001g0004a0001c0001t0001g0129a0001c0001t0001g0143others(45): Show | 49 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.110-17881T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596936 | ||||||
| chr3:139596938
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0078 | 2 | HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.110-17883T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596938 | ||||||
| chr3:139596939
|
TATATATA others(10): Show |
T | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17901_110-1788 others(21): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596939 | ||||||
| chr3:139596940
|
A | G | 4 | a0001c0001t0001g0166a0001c0001t0001g0246a0001c0001t0001g0301others(1): Show | 4 | HG02273.hp1 HG03486.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17885T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596940 | ||||||
| chr3:139596942
|
A | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(69): Show | 73 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(70): Show |
intron_variant | MODIFIER | c.110-17887T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596942 | ||||||
| chr3:139596943
|
TATATATA others(8): Show |
T | 5 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(2): Show | 5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-17903_110-1788 others(19): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596943 | ||||||
| chr3:139596954
|
A | G | 2 | a0001c0001t0001g0256a0002c0006t0001g0254 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.110-17899T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596954 | ||||||
| chr3:139596956
|
ATATATAT others(3): Show |
A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-17911_110-1790 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596956 | ||||||
| chr3:139596958
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.110-17903T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596958 | ||||||
| chr3:139596958
|
A | T | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17903T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596958 | ||||||
| chr3:139596960
|
A | T | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-17905T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596960 | ||||||
| chr3:139596962
|
A | T | 13 | a0001c0001t0001g0189a0001c0001t0002g0001a0001c0001t0002g0043others(10): Show | 14 | HG01175.hp1 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-17907T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596962 | ||||||
| chr3:139596964
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.110-17910_110-1790 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596964 | ||||||
| chr3:139596964
|
A | T | 25 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(22): Show | 26 | HG00280.hp1 HG00733.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.110-17909T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596964 | ||||||
| chr3:139597027
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-17972C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597027 | ||||||
| chr3:139597167
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-18112G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597167 | ||||||
| chr3:139597197
|
T | C | 84 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-18142A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597197 | ||||||
| chr3:139597367
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-18312A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597367 | ||||||
| chr3:139597375
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-18320C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597375 | ||||||
| chr3:139597533
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-18478G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597533 | ||||||
| chr3:139597565
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.110-18510C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597565 | ||||||
| chr3:139597584
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-18529T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597584 | ||||||
| chr3:139597940
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-18885T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597940 | ||||||
| chr3:139597972
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0227 | 2 | HG01243.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.110-18917C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597972 | ||||||
| chr3:139598072
|
A | T | 4 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0039others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-19017T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598072 | ||||||
| chr3:139598164
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110-19109C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598164 | ||||||
| chr3:139598367
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-19312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598367 | ||||||
| chr3:139598377
|
T | C | 21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-19322A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598377 | ||||||
| chr3:139598392
|
T | C | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-19337A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598392 | ||||||
| chr3:139598863
|
T | C | 9 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0125others(6): Show | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-19808A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598863 | ||||||
| chr3:139599131
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-20076T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599131 | ||||||
| chr3:139599252
|
C | T | 3 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0002g0058 | 3 | HG01243.hp2 HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-20197G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599252 | ||||||
| chr3:139599399
|
A | T | 84 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-20344T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599399 | ||||||
| chr3:139599626
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.110-20571G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599626 | ||||||
| chr3:139599818
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-20763G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599818 | ||||||
| chr3:139600131
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-21076T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600131 | ||||||
| chr3:139600182
|
T | C | 1 | a0001c0001t0005g0006 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-21127A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600182 | ||||||
| chr3:139600306
|
A | AT | 43 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0106others(40): Show | 44 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.110-21252dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600306 | ||||||
| chr3:139600430
|
C | T | 82 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-21375G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600430 | ||||||
| chr3:139600518
|
G | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-21463C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600518 | ||||||
| chr3:139600633
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-21578G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600633 | ||||||
| chr3:139600793
|
C | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0275a0001c0001t0001g0293others(6): Show | 10 | HG01192.hp1 HG02165.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-21738G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600793 | ||||||
| chr3:139601155
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-22100A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601155 | ||||||
| chr3:139601248
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-22193C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601248 | ||||||
| chr3:139601760
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-22705A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601760 | ||||||
| chr3:139601795
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-22740C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601795 | ||||||
| chr3:139602080
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0197 | 2 | HG01256.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.110-23025G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602080 | ||||||
| chr3:139602165
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-23110T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602165 | ||||||
| chr3:139602392
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-23337T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602392 | ||||||
| chr3:139602710
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-23655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602710 | ||||||
| chr3:139602820
|
T | C | 17 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 17 | HG01099.hp2 HG01433.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-23765A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602820 | ||||||
| chr3:139602887
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.110-23832G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602887 | ||||||
| chr3:139603264
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110-24209G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603264 | ||||||
| chr3:139603266
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.110-24211A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603266 | ||||||
| chr3:139603280
|
G | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-24225C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603280 | ||||||
| chr3:139603305
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-24250A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603305 | ||||||
| chr3:139603506
|
C | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 257 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.109+24110G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603506 | ||||||
| chr3:139603524
|
CA | C | 14 | a0001c0001t0001g0126a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+24091delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603524 | ||||||
| chr3:139603613
|
ACCG | A | 18 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0130others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.109+24000_109+2400 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603613 | ||||||
| chr3:139603616
|
G | A | 13 | a0001c0001t0001g0126a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 14 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+24000C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603616 | ||||||
| chr3:139603625
|
G | A | 99 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0126others(96): Show | 100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.109+23991C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603625 | ||||||
| chr3:139603642
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0002g0058 | 2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109+23974C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603642 | ||||||
| chr3:139603743
|
A | C | 67 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0107others(64): Show | 67 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.109+23873T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603743 | ||||||
| chr3:139603805
|
AC | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0110others(14): Show | 17 | HG01123.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+23810delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603805 | ||||||
| chr3:139604032
|
G | T | 21 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0121others(18): Show | 21 | HG01123.hp1 HG01175.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.109+23584C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604032 | ||||||
| chr3:139604118
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+23498G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604118 | ||||||
| chr3:139604206
|
C | G | 1 | a0001c0007t0001g0255 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.109+23410G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604206 | ||||||
| chr3:139604310
|
A | C | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0179others(4): Show | 7 | HG01123.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+23306T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604310 | ||||||
| chr3:139604476
|
T | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+23140A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604476 | ||||||
| chr3:139604521
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.109+23095C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604521 | ||||||
| chr3:139604672
|
A | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0051 | 4 | HG01257.hp1 HG01258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+22944T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604672 | ||||||
| chr3:139604739
|
T | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+22877A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604739 | ||||||
| chr3:139604818
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0211 | 2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.109+22798A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604818 | ||||||
| chr3:139604839
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.109+22777A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604839 | ||||||
| chr3:139604910
|
G | A | 80 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 81 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.109+22706C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604910 | ||||||
| chr3:139605040
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+22576T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605040 | ||||||
| chr3:139605043
|
AC | A | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+22572delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605043 | ||||||
| chr3:139605073
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+22543C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605073 | ||||||
| chr3:139605149
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.109+22467C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605149 | ||||||
| chr3:139605617
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0018 | 3 | HG01257.hp1 HG01258.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.109+21999G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605617 | ||||||
| chr3:139605771
|
T | G | 30 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(27): Show | 30 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.109+21845A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605771 | ||||||
| chr3:139605914
|
AT | A | 50 | a0001c0001t0001g0117a0001c0001t0001g0119a0001c0001t0001g0130others(47): Show | 50 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.109+21701delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | ||||||
| chr3:139605914
|
ATT | A | 255 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0098others(252): Show | 259 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.109+21700_109+2170 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | ||||||
| chr3:139605914
|
ATTT | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0137a0001c0001t0001g0143others(3): Show | 7 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+21699_109+2170 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | ||||||
| chr3:139605995
|
A | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0098a0001c0001t0001g0099others(74): Show | 78 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.109+21621T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605995 | ||||||
| chr3:139606162
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+21454G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606162 | ||||||
| chr3:139606187
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.109+21429T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606187 | ||||||
| chr3:139606258
|
C | G | 6 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0157others(3): Show | 6 | HG02015.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+21358G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606258 | ||||||
| chr3:139606514
|
G | C | 17 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(14): Show | 17 | HG01243.hp1 HG01433.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+21102C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606514 | ||||||
| chr3:139606642
|
A | G | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.109+20974T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606642 | ||||||
| chr3:139606903
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+20713C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606903 | ||||||
| chr3:139606990
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+20626G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606990 | ||||||
| chr3:139607215
|
T | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 271 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.109+20401A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607215 | ||||||
| chr3:139607310
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+20306G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607310 | ||||||
| chr3:139607642
|
T | C | 139 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0106others(136): Show | 142 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.109+19974A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607642 | ||||||
| chr3:139607663
|
G | GT | 293 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(290): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.109+19952dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607663 | ||||||
| chr3:139607684
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+19932A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607684 | ||||||
| chr3:139608024
|
A | T | 1 | a0001c0001t0001g0274 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.109+19592T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608024 | ||||||
| chr3:139608176
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.109+19440G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608176 | ||||||
| chr3:139608332
|
TAACA | T | 278 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.109+19280_109+1928 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608332 | ||||||
| chr3:139608419
|
A | G | 211 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0106others(208): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.109+19197T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608419 | ||||||
| chr3:139608494
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+19122G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608494 | ||||||
| chr3:139608882
|
C | T | 3 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0029 | 3 | HG00639.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.109+18734G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608882 | ||||||
| chr3:139608895
|
G | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(279): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.109+18721C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608895 | ||||||
| chr3:139609130
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+18486G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609130 | ||||||
| chr3:139609385
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+18231G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609385 | ||||||
| chr3:139609538
|
C | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(44): Show | 48 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.109+18078G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609538 | ||||||
| chr3:139609546
|
G | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+18070C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609546 | ||||||
| chr3:139609563
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+18053C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609563 | ||||||
| chr3:139609582
|
T | TTTAA | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+18033_109+1803 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609582 | ||||||
| chr3:139609633
|
G | A | 18 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 18 | HG01433.hp2 HG02602.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.109+17983C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609633 | ||||||
| chr3:139609657
|
G | GT | 187 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.109+17958dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609657 | ||||||
| chr3:139609667
|
T | TC | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(93): Show | 99 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.109+17948_109+1794 others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609667 | ||||||
| chr3:139609872
|
A | G | 1 | a0001c0001t0002g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.109+17744T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609872 | ||||||
| chr3:139609892
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+17724A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609892 | ||||||
| chr3:139609897
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+17719G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609897 | ||||||
| chr3:139610001
|
T | C | 1 | a0001c0001t0002g0057 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.109+17615A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610001 | ||||||
| chr3:139610070
|
G | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+17546C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610070 | ||||||
| chr3:139610499
|
A | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+17117T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610499 | ||||||
| chr3:139610509
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+17107G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610509 | ||||||
| chr3:139610606
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+17010T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610606 | ||||||
| chr3:139610738
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16878A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610738 | ||||||
| chr3:139610764
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16852A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610764 | ||||||
| chr3:139610773
|
A | G | 1 | a0001c0001t0002g0038 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109+16843T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610773 | ||||||
| chr3:139610821
|
C | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16795G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610821 | ||||||
| chr3:139610844
|
C | T | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+16772G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610844 | ||||||
| chr3:139611035
|
TGGG | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16578_109+1658 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611035 | ||||||
| chr3:139611047
|
T | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16569A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611047 | ||||||
| chr3:139611096
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+16520A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611096 | ||||||
| chr3:139611137
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.109+16479G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611137 | ||||||
| chr3:139611194
|
T | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+16422A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611194 | ||||||
| chr3:139611517
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+16099A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611517 | ||||||
| chr3:139611561
|
T | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.109+16055A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611561 | ||||||
| chr3:139611753
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15863T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611753 | ||||||
| chr3:139611761
|
C | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(44): Show | 48 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.109+15855G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611761 | ||||||
| chr3:139611762
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.109+15854C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611762 | ||||||
| chr3:139611785
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+15831T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611785 | ||||||
| chr3:139611817
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15799T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611817 | ||||||
| chr3:139611851
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0002g0052 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+15765A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611851 | ||||||
| chr3:139611884
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15732C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611884 | ||||||
| chr3:139611899
|
T | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.109+15717A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611899 | ||||||
| chr3:139611951
|
G | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15665C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611951 | ||||||
| chr3:139611958
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+15658C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611958 | ||||||
| chr3:139611974
|
C | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15642G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611974 | ||||||
| chr3:139612036
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15580C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612036 | ||||||
| chr3:139612102
|
A | G | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.109+15514T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612102 | ||||||
| chr3:139612120
|
CTG | C | 13 | a0001c0001t0001g0216a0001c0001t0001g0261a0001c0001t0001g0296others(10): Show | 13 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+15494_109+1549 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612120 | ||||||
| chr3:139612135
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+15481G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612135 | ||||||
| chr3:139612167
|
C | CA | 151 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(148): Show | 153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.109+15448dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | ||||||
| chr3:139612167
|
C | CAA | 8 | a0001c0001t0001g0123a0001c0001t0001g0165a0001c0001t0001g0168others(5): Show | 8 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+15447_109+1544 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | ||||||
| chr3:139612167
|
CA | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0101others(69): Show | 75 | HG00423.hp2 HG00438.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.109+15448delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | ||||||
| chr3:139612219
|
G | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(114): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+15397C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612219 | ||||||
| chr3:139612255
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15361C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612255 | ||||||
| chr3:139612384
|
T | C | 1 | a0001c0001t0012g0262 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.109+15232A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612384 | ||||||
| chr3:139612452
|
T | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.109+15164A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612452 | ||||||
| chr3:139612550
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.109+15066A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612550 | ||||||
| chr3:139612618
|
A | C | 4 | a0001c0001t0001g0106a0001c0001t0002g0008a0001c0001t0002g0009others(1): Show | 4 | HG01099.hp2 HG01109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+14998T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612618 | ||||||
| chr3:139612803
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+14813T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612803 | ||||||
| chr3:139612999
|
A | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0250 | 2 | NA18941.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.109+14617T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612999 | ||||||
| chr3:139613120
|
A | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.109+14496T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613120 | ||||||
| chr3:139613139
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14477G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613139 | ||||||
| chr3:139613193
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14423C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613193 | ||||||
| chr3:139613205
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14411C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613205 | ||||||
| chr3:139613206
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14410T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613206 | ||||||
| chr3:139613213
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14403A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613213 | ||||||
| chr3:139613222
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14394A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613222 | ||||||
| chr3:139613227
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14389A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613227 | ||||||
| chr3:139613253
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14363G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613253 | ||||||
| chr3:139613256
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14360C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613256 | ||||||
| chr3:139613356
|
T | C | 11 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+14260A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613356 | ||||||
| chr3:139613411
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.109+14205T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613411 | ||||||
| chr3:139613448
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.109+14168G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613448 | ||||||
| chr3:139613456
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14160C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613456 | ||||||
| chr3:139613506
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+14110C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613506 | ||||||
| chr3:139613514
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14102G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613514 | ||||||
| chr3:139613529
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.109+14087A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613529 | ||||||
| chr3:139613542
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.109+14074C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613542 | ||||||
| chr3:139613592
|
C | G | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+14024G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613592 | ||||||
| chr3:139613642
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(114): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+13974G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613642 | ||||||
| chr3:139613675
|
C | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0261a0001c0001t0001g0296 | 3 | NA18961.hp1 NA19065.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.109+13941G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613675 | ||||||
| chr3:139613725
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+13891C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613725 | ||||||
| chr3:139613785
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0287others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+13831G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613785 | ||||||
| chr3:139613867
|
C | T | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109+13749G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613867 | ||||||
| chr3:139613903
|
C | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+13713G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613903 | ||||||
| chr3:139613946
|
A | G | 10 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+13670T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613946 | ||||||
| chr3:139613961
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109+13655C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613961 | ||||||
| chr3:139614001
|
G | C | 2 | a0001c0001t0001g0118a0001c0001t0006g0048 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.109+13615C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614001 | ||||||
| chr3:139614003
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+13613C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614003 | ||||||
| chr3:139614042
|
C | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+13574G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614042 | ||||||
| chr3:139614224
|
C | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+13392G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614224 | ||||||
| chr3:139614241
|
T | TA | 5 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0200others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+13374dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614241 | ||||||
| chr3:139614256
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+13360G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614256 | ||||||
| chr3:139614539
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+13077G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614539 | ||||||
| chr3:139614654
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12962A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614654 | ||||||
| chr3:139614671
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+12945C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614671 | ||||||
| chr3:139614768
|
G | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+12848C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614768 | ||||||
| chr3:139614823
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12793C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614823 | ||||||
| chr3:139614961
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+12655A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614961 | ||||||
| chr3:139615081
|
C | G | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(13): Show | 16 | HG01433.hp2 HG02615.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+12535G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615081 | ||||||
| chr3:139615189
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.109+12427G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615189 | ||||||
| chr3:139615415
|
T | TTCTATCT others(3): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0209 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.109+12200_109+1220 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615415 | ||||||
| chr3:139615417
|
T | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0209 | 2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.109+12199A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTA | 80 | a0001c0001t0001g0004a0001c0001t0001g0098a0001c0001t0001g0099others(77): Show | 82 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.109+12195_109+1219 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(1): Show |
87 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0121others(84): Show | 88 | HG00438.hp2 HG00621.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.109+12191_109+1219 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(5): Show |
61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0129others(58): Show | 63 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.109+12187_109+1219 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(9): Show |
42 | a0001c0001t0001g0107a0001c0001t0001g0119a0001c0001t0001g0128others(39): Show | 42 | HG00323.hp1 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+12183_109+1219 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(13): Show |
10 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0240others(7): Show | 10 | HG00438.hp1 HG02155.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+12179_109+1219 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(17): Show |
3 | a0001c0001t0001g0161a0001c0001t0001g0219a0001c0001t0001g0233 | 3 | HG02080.hp2 HG02523.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.109+12175_109+1219 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615417
|
T | TTCTATCT others(13): Show |
1 | a0001c0001t0001g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.109+12198_109+1219 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | ||||||
| chr3:139615460
|
T | TATCTATC others(9): Show |
1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+12155_109+1215 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615460 | ||||||
| chr3:139615464
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0263 | 2 | HG01243.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.109+12152G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615464 | ||||||
| chr3:139615466
|
TCCAC | T | 134 | a0001c0001t0001g0005a0001c0001t0001g0100a0001c0001t0001g0101others(131): Show | 136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.109+12146_109+1214 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615466 | ||||||
| chr3:139615470
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0106others(147): Show | 153 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.109+12146G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615470 | ||||||
| chr3:139615474
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+12142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615474 | ||||||
| chr3:139615478
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+12138A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615478 | ||||||
| chr3:139615507
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12109G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615507 | ||||||
| chr3:139615650
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0018a0001c0001t0002g0051 | 4 | HG01257.hp1 HG01258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+11966A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615650 | ||||||
| chr3:139615724
|
G | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+11892C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615724 | ||||||
| chr3:139615725
|
CGTGT | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+11887_109+1189 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615725 | ||||||
| chr3:139615827
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.109+11789G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615827 | ||||||
| chr3:139615867
|
TTG | T | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+11747_109+1174 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615867 | ||||||
| chr3:139615874
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+11742C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615874 | ||||||
| chr3:139616164
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0199others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+11452G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616164 | ||||||
| chr3:139616268
|
T | C | 13 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0179others(10): Show | 13 | HG01123.hp1 HG01175.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+11348A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616268 | ||||||
| chr3:139616270
|
A | T | 1 | a0001c0001t0002g0079 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.109+11346T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616270 | ||||||
| chr3:139616523
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+11093T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616523 | ||||||
| chr3:139616536
|
A | T | 4 | a0001c0001t0001g0106a0001c0001t0002g0008a0001c0001t0002g0009others(1): Show | 4 | HG01099.hp2 HG01109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+11080T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616536 | ||||||
| chr3:139616661
|
T | G | 1 | a0001c0001t0001g0264 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.109+10955A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616661 | ||||||
| chr3:139616774
|
C | G | 2 | a0001c0001t0001g0272a0001c0001t0002g0039 | 2 | HG02080.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.109+10842G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616774 | ||||||
| chr3:139616776
|
G | C | 1 | a0001c0001t0002g0002 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.109+10840C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616776 | ||||||
| chr3:139616806
|
G | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0293 | 2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.109+10810C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616806 | ||||||
| chr3:139616821
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+10795G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616821 | ||||||
| chr3:139616851
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+10765A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616851 | ||||||
| chr3:139617253
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+10363T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617253 | ||||||
| chr3:139617321
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0109 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.109+10295C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617321 | ||||||
| chr3:139617444
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(114): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+10172G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617444 | ||||||
| chr3:139617539
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109+10077A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617539 | ||||||
| chr3:139617539
|
T | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0106others(145): Show | 151 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.109+10077A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617539 | ||||||
| chr3:139617555
|
C | T | 2 | a0001c0001t0001g0163a0001c0004t0001g0147 | 2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.109+10061G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617555 | ||||||
| chr3:139617593
|
T | C | 1 | a0001c0001t0001g0004 | 2 | NA18950.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.109+10023A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617593 | ||||||
| chr3:139617902
|
T | C | 40 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0131others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.109+9714A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617902 | ||||||
| chr3:139618478
|
G | GGAAA | 10 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+9134_109+9137d others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618478 | ||||||
| chr3:139618770
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109+8846T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618770 | ||||||
| chr3:139618864
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0226 | 2 | NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.109+8752T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618864 | ||||||
| chr3:139618957
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109+8659C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618957 | ||||||
| chr3:139619285
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109+8331C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619285 | ||||||
| chr3:139619400
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.109+8216A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619400 | ||||||
| chr3:139619781
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0002g0072 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.109+7835G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619781 | ||||||
| chr3:139619787
|
A | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+7829T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619787 | ||||||
| chr3:139619873
|
T | C | 1 | a0001c0001t0009g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.109+7743A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619873 | ||||||
| chr3:139619922
|
A | C | 14 | a0001c0001t0001g0123a0001c0001t0001g0164a0001c0001t0001g0165others(11): Show | 14 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+7694T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619922 | ||||||
| chr3:139620028
|
AT | A | 36 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.109+7587delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620028 | ||||||
| chr3:139620103
|
T | G | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+7513A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620103 | ||||||
| chr3:139620136
|
G | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(96): Show | 102 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(99): Show |
intron_variant | MODIFIER | c.109+7480C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620136 | ||||||
| chr3:139620156
|
G | C | 1 | a0001c0001t0002g0077 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.109+7460C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620156 | ||||||
| chr3:139620200
|
C | CT | 31 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(28): Show | 31 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.109+7415dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | ||||||
| chr3:139620200
|
C | CTT | 41 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0131others(38): Show | 41 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.109+7414_109+7415d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | ||||||
| chr3:139620200
|
CT | C | 9 | a0001c0001t0001g0098a0001c0001t0001g0110a0001c0001t0001g0119others(6): Show | 9 | HG01169.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+7415delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | ||||||
| chr3:139620254
|
C | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0180a0001c0002t0001g0175 | 3 | HG02895.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.109+7362G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620254 | ||||||
| chr3:139620767
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+6849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620767 | ||||||
| chr3:139620771
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+6845A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620771 | ||||||
| chr3:139620820
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.109+6796C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620820 | ||||||
| chr3:139620956
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.109+6660C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620956 | ||||||
| chr3:139621058
|
C | T | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+6558G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621058 | ||||||
| chr3:139621135
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+6481A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621135 | ||||||
| chr3:139621176
|
G | A | 11 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(8): Show | 11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+6440C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621176 | ||||||
| chr3:139621294
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.109+6322A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621294 | ||||||
| chr3:139621304
|
T | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0100others(103): Show | 109 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(106): Show |
intron_variant | MODIFIER | c.109+6312A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621304 | ||||||
| chr3:139621305
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.109+6311A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621305 | ||||||
| chr3:139621386
|
T | C | 10 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+6230A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621386 | ||||||
| chr3:139621394
|
C | T | 6 | a0001c0001t0001g0121a0001c0001t0001g0178a0001c0001t0001g0191others(3): Show | 6 | HG01433.hp2 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+6222G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621394 | ||||||
| chr3:139621612
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+6004A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621612 | ||||||
| chr3:139621876
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+5740G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621876 | ||||||
| chr3:139621972
|
C | G | 1 | a0001c0001t0001g0298 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.109+5644G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621972 | ||||||
| chr3:139622054
|
G | T | 36 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.109+5562C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622054 | ||||||
| chr3:139622070
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.109+5546A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622070 | ||||||
| chr3:139622376
|
AT | A | 39 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0001g0131others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.109+5239delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622376 | ||||||
| chr3:139622420
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0002g0052 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+5196C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622420 | ||||||
| chr3:139622452
|
ACGCCAG | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0116others(114): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+5158_109+5163d others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622452 | ||||||
| chr3:139622501
|
G | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+5115C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622501 | ||||||
| chr3:139622576
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0110others(93): Show | 99 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.109+5040A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622576 | ||||||
| chr3:139622578
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+5038G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622578 | ||||||
| chr3:139622722
|
A | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+4894T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622722 | ||||||
| chr3:139622768
|
T | G | 1 | a0001c0001t0002g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.109+4848A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622768 | ||||||
| chr3:139622771
|
C | CATATATA others(4): Show |
6 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG00738.hp2 HG01106.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+4834_109+4844d others(13): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622771 | ||||||
| chr3:139622780
|
G | T | 2 | a0001c0001t0001g0170a0001c0001t0002g0052 | 2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+4836C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622780 | ||||||
| chr3:139622817
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+4799A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622817 | ||||||
| chr3:139622848
|
T | TTA | 64 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0101others(61): Show | 66 | HG00738.hp2 HG01106.hp1 HG01169.hp2 others(63): Show |
intron_variant | MODIFIER | c.109+4766_109+4767d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622848 | ||||||
| chr3:139622848
|
T | TTATA | 48 | a0001c0001t0001g0004a0001c0001t0001g0127a0001c0001t0001g0159others(45): Show | 49 | HG00423.hp2 HG00438.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.109+4764_109+4767d others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622848 | ||||||
| chr3:139622850
|
A | T | 4 | a0001c0001t0001g0182a0001c0001t0001g0201a0001c0001t0002g0008others(1): Show | 4 | HG02572.hp1 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+4766T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622850 | ||||||
| chr3:139622865
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0004g0096a0001c0001t0004g0097 | 3 | HG01081.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.109+4751A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622865 | ||||||
| chr3:139622941
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0307 | 3 | NA18966.hp2 NA19004.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.109+4675C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622941 | ||||||
| chr3:139622962
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+4654G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622962 | ||||||
| chr3:139622964
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+4652C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622964 | ||||||
| chr3:139623241
|
T | C | 157 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.109+4375A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623241 | ||||||
| chr3:139623335
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0186 | 2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.109+4281C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623335 | ||||||
| chr3:139623373
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.109+4243A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623373 | ||||||
| chr3:139623486
|
G | T | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+4130C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623486 | ||||||
| chr3:139623531
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.109+4085G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623531 | ||||||
| chr3:139623583
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+4033C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623583 | ||||||
| chr3:139623622
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.109+3994G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623622 | ||||||
| chr3:139623647
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+3969T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623647 | ||||||
| chr3:139623699
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+3917C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623699 | ||||||
| chr3:139623736
|
C | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0296 | 2 | NA18961.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.109+3880G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623736 | ||||||
| chr3:139623745
|
G | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+3871C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623745 | ||||||
| chr3:139623848
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.109+3768A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623848 | ||||||
| chr3:139623969
|
C | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.109+3647G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623969 | ||||||
| chr3:139624191
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+3425C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624191 | ||||||
| chr3:139624451
|
C | CT | 8 | a0001c0001t0001g0219a0001c0001t0001g0225a0001c0001t0001g0259others(5): Show | 8 | HG00423.hp2 HG02145.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+3164dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624451 | ||||||
| chr3:139624510
|
C | T | 9 | a0001c0001t0001g0183a0001c0001t0001g0205a0001c0001t0001g0206others(6): Show | 9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+3106G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624510 | ||||||
| chr3:139624637
|
C | T | 2 | a0001c0001t0001g0106a0004c0008t0001g0160 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.109+2979G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624637 | ||||||
| chr3:139624657
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.109+2959G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624657 | ||||||
| chr3:139624747
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+2869G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624747 | ||||||
| chr3:139624887
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+2729T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624887 | ||||||
| chr3:139624940
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+2676A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624940 | ||||||
| chr3:139624997
|
T | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0100others(105): Show | 111 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(108): Show |
intron_variant | MODIFIER | c.109+2619A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624997 | ||||||
| chr3:139625799
|
A | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+1817T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625799 | ||||||
| chr3:139625817
|
G | A | 14 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0178others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+1799C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625817 | ||||||
| chr3:139625886
|
C | T | 21 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0145others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+1730G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625886 | ||||||
| chr3:139625887
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+1729C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625887 | ||||||
| chr3:139626012
|
G | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+1604C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626012 | ||||||
| chr3:139626029
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+1587A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626029 | ||||||
| chr3:139626193
|
A | T | 1 | a0001c0001t0002g0042 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109+1423T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626193 | ||||||
| chr3:139626356
|
C | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+1260G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626356 | ||||||
| chr3:139626361
|
C | A | 156 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(153): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.109+1255G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626361 | ||||||
| chr3:139626628
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.109+988A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626628 | ||||||
| chr3:139626752
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.109+864A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626752 | ||||||
| chr3:139626766
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+850A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626766 | ||||||
| chr3:139627155
|
G | T | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+461C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139627155 | ||||||
| chr3:139627572
|
T | C | 1 | a0001c0001t0006g0048 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+44A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139627572 | ||||||
| chr3:139627800
|
G | A | 1 | a0002c0006t0001g0254 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-40-36C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139627800 | ||||||
| chr3:139627842
|
C | G | 70 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(67): Show | 71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-40-78G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139627842 | ||||||
| chr3:139628032
|
C | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0074others(1): Show | 4 | HG00741.hp1 HG02300.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-268G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628032 | ||||||
| chr3:139628214
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-40-450A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628214 | ||||||
| chr3:139628296
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-532G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628296 | ||||||
| chr3:139628343
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-579G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628343 | ||||||
| chr3:139628448
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-684A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628448 | ||||||
| chr3:139628516
|
A | G | 71 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(68): Show | 72 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-40-752T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628516 | ||||||
| chr3:139628626
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-862T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628626 | ||||||
| chr3:139628871
|
C | T | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-40-1107G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628871 | ||||||
| chr3:139629023
|
G | A | 1 | a0001c0001t0004g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-40-1259C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629023 | ||||||
| chr3:139629280
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-40-1516C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629280 | ||||||
| chr3:139629310
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-1546C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629310 | ||||||
| chr3:139629331
|
C | T | 14 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0178others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-1567G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629331 | ||||||
| chr3:139629566
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-40-1802G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629566 | ||||||
| chr3:139629593
|
A | T | 1 | a0001c0001t0001g0293 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-40-1829T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629593 | ||||||
| chr3:139629676
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 226 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-40-1912A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629676 | ||||||
| chr3:139629727
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-1963A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629727 | ||||||
| chr3:139629836
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40-2072G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629836 | ||||||
| chr3:139629915
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-40-2151C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629915 | ||||||
| chr3:139630417
|
G | C | 15 | a0001c0001t0001g0163a0001c0001t0001g0188a0001c0001t0001g0189others(12): Show | 16 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40-2653C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630417 | ||||||
| chr3:139630425
|
G | T | 1 | a0001c0001t0001g0004 | 2 | NA18950.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-40-2661C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630425 | ||||||
| chr3:139630475
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-2711T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630475 | ||||||
| chr3:139630477
|
C | T | 1 | a0001c0001t0002g0025 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-40-2713G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630477 | ||||||
| chr3:139630561
|
C | A | 1 | a0001c0001t0004g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-2797G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630561 | ||||||
| chr3:139630580
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-2816G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630580 | ||||||
| chr3:139630581
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-40-2817C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630581 | ||||||
| chr3:139630701
|
C | T | 10 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0023others(7): Show | 10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-2937G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630701 | ||||||
| chr3:139630766
|
C | A | 1 | a0001c0001t0002g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-40-3002G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630766 | ||||||
| chr3:139631090
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-40-3326C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631090 | ||||||
| chr3:139631146
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-40-3382C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631146 | ||||||
| chr3:139631191
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-41+3420G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631191 | ||||||
| chr3:139631466
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+3145C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631466 | ||||||
| chr3:139631474
|
T | C | 73 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(70): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-41+3137A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631474 | ||||||
| chr3:139631537
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-41+3074C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631537 | ||||||
| chr3:139631546
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-41+3065C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631546 | ||||||
| chr3:139631577
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-41+3034C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631577 | ||||||
| chr3:139631810
|
C | T | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+2801G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631810 | ||||||
| chr3:139631811
|
C | G | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(219): Show | 227 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-41+2800G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631811 | ||||||
| chr3:139631818
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+2793G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631818 | ||||||
| chr3:139631852
|
T | C | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+2759A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631852 | ||||||
| chr3:139631875
|
T | G | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(7): Show | 10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+2736A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631875 | ||||||
| chr3:139631898
|
T | A | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-41+2713A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631898 | ||||||
| chr3:139631912
|
C | G | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-41+2699G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631912 | ||||||
| chr3:139631929
|
T | C | 54 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0107others(51): Show | 55 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-41+2682A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631929 | ||||||
| chr3:139632349
|
A | G | 22 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(19): Show | 22 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-41+2262T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632349 | ||||||
| chr3:139632357
|
C | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0126others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-41+2254G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632357 | ||||||
| chr3:139632464
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41+2147C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632464 | ||||||
| chr3:139632538
|
G | A | 5 | a0001c0001t0001g0178a0001c0003t0001g0193a0001c0003t0002g0061others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+2073C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632538 | ||||||
| chr3:139632815
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194 | 3 | HG02717.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-41+1796C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632815 | ||||||
| chr3:139632843
|
T | C | 11 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+1768A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632843 | ||||||
| chr3:139632856
|
G | A | 11 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+1755C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632856 | ||||||
| chr3:139632962
|
C | T | 53 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(50): Show | 54 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-41+1649G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632962 | ||||||
| chr3:139633040
|
C | A | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+1571G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633040 | ||||||
| chr3:139633055
|
G | A | 1 | a0001c0001t0001g0314 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-41+1556C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633055 | ||||||
| chr3:139633063
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-41+1548C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633063 | ||||||
| chr3:139633064
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-41+1547G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633064 | ||||||
| chr3:139633078
|
G | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 201 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-41+1533C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633078 | ||||||
| chr3:139633114
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-41+1497C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633114 | ||||||
| chr3:139633180
|
G | GA | 82 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(79): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-41+1430dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633180 | ||||||
| chr3:139633181
|
A | AT | 21 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0132others(18): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-41+1429dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633181 | ||||||
| chr3:139633181
|
AT | A | 23 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0126others(20): Show | 23 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41+1429delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633181 | ||||||
| chr3:139633182
|
T | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0002g0075 | 3 | HG02155.hp2 HG03491.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-41+1429A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633182 | ||||||
| chr3:139633212
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-41+1399G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633212 | ||||||
| chr3:139633257
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-41+1354G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633257 | ||||||
| chr3:139633261
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(82): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+1350C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633261 | ||||||
| chr3:139633328
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-41+1283C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633328 | ||||||
| chr3:139633369
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-41+1242C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633369 | ||||||
| chr3:139633455
|
C | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+1156G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633455 | ||||||
| chr3:139633566
|
T | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+1045A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633566 | ||||||
| chr3:139633724
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-41+887A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633724 | ||||||
| chr3:139634349
|
C | A | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+262G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139634349 | ||||||
| chr3:139634533
|
C | T | 11 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126others(8): Show | 11 | HG01243.hp1 HG01496.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+78G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139634533 | ||||||
| chr3:139634764
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-77-117G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634764 | ||||||
| chr3:139634765
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-118C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634765 | ||||||
| chr3:139634822
|
A | G | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-77-175T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634822 | ||||||
| chr3:139634867
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-77-220A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634867 | ||||||
| chr3:139634901
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-77-254A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634901 | ||||||
| chr3:139635135
|
A | G | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-77-488T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635135 | ||||||
| chr3:139635143
|
T | C | 1 | a0001c0001t0001g0302 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-77-496A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635143 | ||||||
| chr3:139635192
|
A | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-77-545T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635192 | ||||||
| chr3:139635400
|
G | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-77-753C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635400 | ||||||
| chr3:139635414
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-77-767C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635414 | ||||||
| chr3:139635438
|
A | G | 4 | a0001c0002t0002g0040a0001c0002t0002g0045a0001c0002t0002g0046others(1): Show | 4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77-791T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635438 | ||||||
| chr3:139635531
|
G | A | 2 | a0001c0001t0001g0186a0004c0008t0001g0160 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-884C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635531 | ||||||
| chr3:139635564
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-917T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635564 | ||||||
| chr3:139635597
|
GA | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126others(1): Show | 4 | HG01243.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-951delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635597 | ||||||
| chr3:139635729
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0002g0053others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-1082A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635729 | ||||||
| chr3:139636004
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-77-1357A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636004 | ||||||
| chr3:139636150
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-77-1503A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636150 | ||||||
| chr3:139636163
|
G | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-1516C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636163 | ||||||
| chr3:139636205
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-77-1558A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636205 | ||||||
| chr3:139636303
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-77-1656G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636303 | ||||||
| chr3:139636335
|
GA | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(67): Show | 73 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-78+1627delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636335 | ||||||
| chr3:139636420
|
A | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-78+1543T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636420 | ||||||
| chr3:139636660
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-78+1303C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636660 | ||||||
| chr3:139636685
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-78+1278T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636685 | ||||||
| chr3:139636826
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-78+1137G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636826 | ||||||
| chr3:139637360
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0002g0065a0001c0001t0002g0081 | 3 | NA18957.hp2 NA18975.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-78+603A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637360 | ||||||
| chr3:139637446
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0036 | 2 | HG01496.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-78+517G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637446 | ||||||
| chr3:139637749
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-78+214G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637749 | ||||||
| chr3:139637923
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(57): Show | 63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-78+40C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637923 | ||||||
| chr3:139637954
|
G | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(77): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-78+9C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637954 | ||||||
| chr3:139638216
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177-154G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638216 | ||||||
| chr3:139638251
|
G | A | 175 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-177-189C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638251 | ||||||
| chr3:139638269
|
G | T | 3 | a0001c0001t0001g0202a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | NA18964.hp1 NA19005.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-177-207C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638269 | ||||||
| chr3:139638396
|
A | C | 2 | a0001c0001t0002g0020a0001c0001t0005g0007 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177-334T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638396 | ||||||
| chr3:139638402
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-340C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638402 | ||||||
| chr3:139638410
|
T | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0227a0001c0001t0001g0244others(8): Show | 12 | HG01192.hp1 HG02165.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177-348A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638410 | ||||||
| chr3:139638457
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-395C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638457 | ||||||
| chr3:139638495
|
G | T | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-177-433C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638495 | ||||||
| chr3:139638537
|
GC | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-476delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638537 | ||||||
| chr3:139638576
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-177-514C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638576 | ||||||
| chr3:139638685
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-623A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638685 | ||||||
| chr3:139638999
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(61): Show | 67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-937T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638999 | ||||||
| chr3:139639081
|
C | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-1019G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639081 | ||||||
| chr3:139639162
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-177-1100G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639162 | ||||||
| chr3:139639311
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1249C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639311 | ||||||
| chr3:139639366
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0001g0211 | 2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-177-1304C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639366 | ||||||
| chr3:139639382
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-1320C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639382 | ||||||
| chr3:139639396
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(61): Show | 67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1334T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639396 | ||||||
| chr3:139639415
|
A | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(61): Show | 67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1353T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639415 | ||||||
| chr3:139639484
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1422C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639484 | ||||||
| chr3:139639504
|
G | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(61): Show | 67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1442C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639504 | ||||||
| chr3:139639715
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1653G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639715 | ||||||
| chr3:139639912
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1850G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639912 | ||||||
| chr3:139640140
|
G | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-2078C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640140 | ||||||
| chr3:139640140
|
G | T | 1 | a0001c0001t0002g0078 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-177-2078C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640140 | ||||||
| chr3:139640193
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-177-2131C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640193 | ||||||
| chr3:139640568
|
T | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-177-2506A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640568 | ||||||
| chr3:139640667
|
C | T | 2 | a0001c0001t0001g0186a0004c0008t0001g0160 | 2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-177-2605G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640667 | ||||||
| chr3:139640691
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(61): Show | 67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-2629T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640691 | ||||||
| chr3:139640737
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-177-2675G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640737 | ||||||
| chr3:139640872
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-2810C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640872 | ||||||
| chr3:139640965
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2903T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640965 | ||||||
| chr3:139640970
|
T | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2908A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640970 | ||||||
| chr3:139640971
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2909T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640971 | ||||||
| chr3:139640972
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2910T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640972 | ||||||
| chr3:139640974
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2912G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640974 | ||||||
| chr3:139640978
|
A | AATTATAT others(15): Show |
1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2917_-177-291 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640978 | ||||||
| chr3:139640996
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2934A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640996 | ||||||
| chr3:139640997
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2935T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640997 | ||||||
| chr3:139641000
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2938G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641000 | ||||||
| chr3:139641003
|
GAACGGTA others(18): Show |
G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2966_-177-294 others(29): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641003 | ||||||
| chr3:139641029
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2967T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641029 | ||||||
| chr3:139641037
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2975G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641037 | ||||||
| chr3:139641081
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3019G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641081 | ||||||
| chr3:139641183
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-177-3121T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641183 | ||||||
| chr3:139641223
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-177-3161A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641223 | ||||||
| chr3:139641383
|
G | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3321C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641383 | ||||||
| chr3:139641401
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3339G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641401 | ||||||
| chr3:139641599
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3537C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641599 | ||||||
| chr3:139641614
|
A | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3552T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641614 | ||||||
| chr3:139641657
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-177-3595G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641657 | ||||||
| chr3:139641665
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-177-3603A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641665 | ||||||
| chr3:139641743
|
A | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-3681T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641743 | ||||||
| chr3:139642085
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-177-4023G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642085 | ||||||
| chr3:139642101
|
G | A | 1 | a0001c0001t0002g0070 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-177-4039C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642101 | ||||||
| chr3:139642187
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-177-4125A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642187 | ||||||
| chr3:139642210
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-4148T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642210 | ||||||
| chr3:139642227
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-177-4165T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642227 | ||||||
| chr3:139642397
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-4335C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642397 | ||||||
| chr3:139642522
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-4460C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642522 | ||||||
| chr3:139642598
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-177-4536G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642598 | ||||||
| chr3:139642900
|
C | G | 11 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177-4838G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642900 | ||||||
| chr3:139642991
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-177-4929C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642991 | ||||||
| chr3:139643126
|
A | T | 9 | a0001c0001t0001g0269a0001c0001t0001g0280a0001c0001t0001g0312others(6): Show | 9 | HG02523.hp2 NA18612.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-5064T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643126 | ||||||
| chr3:139643297
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-177-5235T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643297 | ||||||
| chr3:139643383
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-177-5321T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643383 | ||||||
| chr3:139643391
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-5329A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643391 | ||||||
| chr3:139643471
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0002g0020 | 2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-5409A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643471 | ||||||
| chr3:139643517
|
C | T | 2 | a0001c0001t0001g0178a0001c0003t0001g0193 | 2 | HG01433.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-177-5455G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643517 | ||||||
| chr3:139643714
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-5652G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643714 | ||||||
| chr3:139643719
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(37): Show | 41 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.-177-5657C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643719 | ||||||
| chr3:139644026
|
C | A | 5 | a0001c0001t0002g0053a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-5964G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644026 | ||||||
| chr3:139644222
|
A | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0002g0053others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-6160T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644222 | ||||||
| chr3:139644226
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-177-6164G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644226 | ||||||
| chr3:139644270
|
A | G | 5 | a0001c0001t0002g0053a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-6208T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644270 | ||||||
| chr3:139644348
|
T | C | 15 | a0001c0001t0001g0163a0001c0001t0001g0188a0001c0001t0001g0189others(12): Show | 16 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-6286A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644348 | ||||||
| chr3:139644465
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-6403G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644465 | ||||||
| chr3:139644601
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177-6539C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644601 | ||||||
| chr3:139644721
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177-6659T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644721 | ||||||
| chr3:139644925
|
C | T | 6 | a0001c0001t0001g0178a0001c0001t0002g0089a0001c0003t0001g0193others(3): Show | 6 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177-6863G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644925 | ||||||
| chr3:139645074
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-177-7012G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645074 | ||||||
| chr3:139645169
|
T | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 5 | HG00738.hp2 HG01106.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-7107A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645169 | ||||||
| chr3:139645337
|
A | G | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-7275T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645337 | ||||||
| chr3:139645374
|
A | G | 1 | a0001c0001t0001g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-177-7312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645374 | ||||||
| chr3:139645464
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(57): Show | 63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-177-7402C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645464 | ||||||
| chr3:139645552
|
C | T | 11 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177-7490G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645552 | ||||||
| chr3:139645564
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-7502C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645564 | ||||||
| chr3:139645764
|
T | C | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-7702A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645764 | ||||||
| chr3:139645833
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-177-7771A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645833 | ||||||
| chr3:139645861
|
C | T | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177-7799G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645861 | ||||||
| chr3:139645862
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-177-7800C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645862 | ||||||
| chr3:139645870
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-177-7808A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645870 | ||||||
| chr3:139645943
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-7881C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645943 | ||||||
| chr3:139646089
|
GGGT | G | 9 | a0001c0001t0001g0161a0001c0001t0001g0263a0001c0001t0001g0264others(6): Show | 9 | HG01255.hp1 HG02523.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-8030_-177-802 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646089 | ||||||
| chr3:139646190
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-8128C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646190 | ||||||
| chr3:139646222
|
A | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0126a0001c0001t0002g0020 | 3 | HG02145.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-8160T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646222 | ||||||
| chr3:139646389
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-8327T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646389 | ||||||
| chr3:139646394
|
T | C | 1 | a0001c0003t0002g0016 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-177-8332A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646394 | ||||||
| chr3:139646439
|
T | C | 1 | a0001c0001t0002g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-177-8377A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646439 | ||||||
| chr3:139646485
|
C | T | 4 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0194others(1): Show | 4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-8423G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646485 | ||||||
| chr3:139646725
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-177-8663C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646725 | ||||||
| chr3:139646837
|
A | C | 1 | a0001c0001t0002g0077 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-177-8775T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646837 | ||||||
| chr3:139646969
|
A | G | 3 | a0001c0001t0001g0295a0001c0001t0002g0019a0001c0001t0002g0076 | 3 | HG02027.hp2 NA18962.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-177-8907T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646969 | ||||||
| chr3:139647152
|
T | C | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(313): Show | 321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-177-9090A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647152 | ||||||
| chr3:139647166
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-177-9104T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647166 | ||||||
| chr3:139647291
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-177-9229A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647291 | ||||||
| chr3:139647300
|
C | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-9238G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647300 | ||||||
| chr3:139647306
|
A | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(58): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-9244T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647306 | ||||||
| chr3:139647487
|
T | C | 18 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0010others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177-9425A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647487 | ||||||
| chr3:139647846
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177-9784A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647846 | ||||||
| chr3:139647849
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-177-9787G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647849 | ||||||
| chr3:139648065
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-10003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648065 | ||||||
| chr3:139648109
|
G | A | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-10047C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648109 | ||||||
| chr3:139648201
|
T | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(59): Show | 64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-10139A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648201 | ||||||
| chr3:139648283
|
T | C | 106 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(103): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-177-10221A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648283 | ||||||
| chr3:139648430
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-177-10368A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648430 | ||||||
| chr3:139648821
|
G | A | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-177-10759C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648821 | ||||||
| chr3:139648917
|
TTATAA | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(56): Show | 61 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-177-10860_-177-10 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648917 | ||||||
| chr3:139649002
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-177-10940T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649002 | ||||||
| chr3:139649002
|
A | G | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-10940T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649002 | ||||||
| chr3:139649204
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0002g0053others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-11142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649204 | ||||||
| chr3:139649211
|
C | A | 7 | a0001c0001t0001g0178a0001c0001t0002g0089a0001c0001t0005g0006others(4): Show | 7 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-11149G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649211 | ||||||
| chr3:139649271
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0123others(60): Show | 65 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-177-11209A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649271 | ||||||
| chr3:139649322
|
A | AAAAC | 40 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0126others(37): Show | 40 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-177-11264_-177-11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | ||||||
| chr3:139649322
|
A | AAAACAAA others(1): Show |
136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0130others(133): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-177-11268_-177-11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | ||||||
| chr3:139649322
|
A | AAAACAAA others(5): Show |
2 | a0001c0001t0002g0041a0001c0001t0002g0049 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-177-11272_-177-11 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | ||||||
| chr3:139649432
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-11370G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649432 | ||||||
| chr3:139649520
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-177-11458T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649520 | ||||||
| chr3:139649762
|
C | G | 1 | a0001c0001t0002g0036 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-177-11700G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649762 | ||||||
| chr3:139649764
|
C | T | 5 | a0001c0001t0001g0210a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01192.hp2 HG01257.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-11702G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649764 | ||||||
| chr3:139649968
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-11906G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649968 | ||||||
| chr3:139650079
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(60): Show | 66 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-177-12017A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650079 | ||||||
| chr3:139650440
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-177-12378T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650440 | ||||||
| chr3:139650717
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-12655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650717 | ||||||
| chr3:139650925
|
T | A | 18 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0010others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177-12863A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650925 | ||||||
| chr3:139651262
|
T | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-13200A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651262 | ||||||
| chr3:139651412
|
A | G | 81 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-177-13350T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651412 | ||||||
| chr3:139651740
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-177-13678C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651740 | ||||||
| chr3:139651812
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-177-13750G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651812 | ||||||
| chr3:139651937
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0110 | 2 | HG01255.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-177-13875C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651937 | ||||||
| chr3:139652122
|
G | A | 7 | a0001c0001t0001g0178a0001c0001t0002g0089a0001c0001t0005g0006others(4): Show | 7 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-14060C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652122 | ||||||
| chr3:139652167
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-14105A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652167 | ||||||
| chr3:139652224
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-14162G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652224 | ||||||
| chr3:139652323
|
A | C | 21 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0164others(18): Show | 21 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-177-14261T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652323 | ||||||
| chr3:139652355
|
T | G | 1 | a0001c0001t0001g0259 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-177-14293A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652355 | ||||||
| chr3:139652753
|
C | T | 8 | a0001c0001t0001g0178a0001c0001t0001g0194a0001c0001t0002g0089others(5): Show | 8 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177-14691G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652753 | ||||||
| chr3:139652923
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-14861C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652923 | ||||||
| chr3:139652924
|
C | T | 5 | a0001c0001t0001g0186a0001c0001t0002g0009a0001c0001t0002g0036others(2): Show | 5 | HG01099.hp2 HG01496.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-14862G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652924 | ||||||
| chr3:139653109
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-15047C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653109 | ||||||
| chr3:139653209
|
A | T | 10 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0205others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-15147T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653209 | ||||||
| chr3:139653313
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0303 | 2 | NA18961.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-177-15251C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653313 | ||||||
| chr3:139653454
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-15392G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653454 | ||||||
| chr3:139653491
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0005g0007 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177-15429T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653491 | ||||||
| chr3:139653576
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-177-15514C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653576 | ||||||
| chr3:139653580
|
C | A | 13 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0181others(10): Show | 13 | HG01099.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.-177-15518G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653580 | ||||||
| chr3:139653681
|
G | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-15619C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653681 | ||||||
| chr3:139653824
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0287others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177-15762C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653824 | ||||||
| chr3:139653834
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-177-15772C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653834 | ||||||
| chr3:139653914
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0121others(85): Show | 91 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-177-15852T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653914 | ||||||
| chr3:139653954
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-177-15892G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653954 | ||||||
| chr3:139654145
|
G | C | 1 | a0001c0001t0001g0279 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-177-16083C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654145 | ||||||
| chr3:139654346
|
G | A | 10 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-16284C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654346 | ||||||
| chr3:139654385
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-177-16323C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654385 | ||||||
| chr3:139654657
|
T | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0273 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-177-16595A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654657 | ||||||
| chr3:139654718
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-177-16656A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654718 | ||||||
| chr3:139654725
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0292a0001c0001t0002g0071 | 3 | HG00621.hp1 NA18747.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-177-16663T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654725 | ||||||
| chr3:139654851
|
C | T | 7 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0002g0053others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-16789G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654851 | ||||||
| chr3:139654870
|
GAC | G | 10 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-16810_-177-16 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654870 | ||||||
| chr3:139654935
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-16873G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654935 | ||||||
| chr3:139655004
|
G | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0110others(1): Show | 4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-16942C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655004 | ||||||
| chr3:139655123
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-17061G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655123 | ||||||
| chr3:139655194
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-177-17132C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655194 | ||||||
| chr3:139655209
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-177-17147C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655209 | ||||||
| chr3:139655209
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-17147C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655209 | ||||||
| chr3:139655261
|
T | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-17199A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655261 | ||||||
| chr3:139655285
|
T | C | 5 | a0001c0001t0002g0053a0001c0002t0002g0040a0001c0002t0002g0045others(2): Show | 5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-17223A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655285 | ||||||
| chr3:139655299
|
C | T | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0178others(9): Show | 12 | HG01123.hp1 HG01243.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177-17237G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655299 | ||||||
| chr3:139655313
|
G | A | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0178others(9): Show | 12 | HG01123.hp1 HG01243.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177-17251C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655313 | ||||||
| chr3:139655626
|
T | TGAA | 202 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(199): Show | 207 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-177-17567_-177-17 others(9): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655626 | ||||||
| chr3:139655696
|
C | T | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-177-17634G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655696 | ||||||
| chr3:139656113
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-177-18051A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656113 | ||||||
| chr3:139656177
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-18115C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656177 | ||||||
| chr3:139656345
|
TCTA | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18286_-177-18 others(9): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656345 | ||||||
| chr3:139656349
|
A | G | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18287T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656349 | ||||||
| chr3:139656351
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(7): Show | 10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18289C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656351 | ||||||
| chr3:139656396
|
C | T | 10 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-18334G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656396 | ||||||
| chr3:139656450
|
G | A | 10 | a0001c0001t0001g0128a0001c0001t0001g0183a0001c0001t0001g0205others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-18388C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656450 | ||||||
| chr3:139656549
|
AG | A | 19 | a0001c0001t0001g0186a0001c0001t0001g0210a0001c0001t0001g0269others(16): Show | 19 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-177-18488delC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656549 | ||||||
| chr3:139656607
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(93): Show | 98 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-177-18545C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656607 | ||||||
| chr3:139656610
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-177-18548T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656610 | ||||||
| chr3:139656650
|
G | T | 7 | a0001c0001t0001g0121a0001c0001t0001g0181a0001c0001t0002g0053others(4): Show | 7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-18588C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656650 | ||||||
| chr3:139656783
|
C | A | 19 | a0001c0001t0001g0186a0001c0001t0001g0210a0001c0001t0001g0269others(16): Show | 19 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-177-18721G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656783 | ||||||
| chr3:139656844
|
AATCTT | A | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG01192.hp2 HG01257.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-177-18787_-177-18 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656844 | ||||||
| chr3:139656846
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-177-18784A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656846 | ||||||
| chr3:139656872
|
T | G | 1 | a0001c0001t0002g0062 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-177-18810A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656872 | ||||||
| chr3:139656909
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-177-18847G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656909 | ||||||
| chr3:139656912
|
G | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-177-18850C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656912 | ||||||
| chr3:139656974
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-18912G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656974 | ||||||
| chr3:139657015
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-177-18953A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657015 | ||||||
| chr3:139657582
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-19520C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657582 | ||||||
| chr3:139657670
|
G | A | 15 | a0001c0001t0001g0210a0001c0001t0001g0269a0001c0001t0001g0280others(12): Show | 15 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-19608C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657670 | ||||||
| chr3:139657688
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-177-19626C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657688 | ||||||
| chr3:139657858
|
AGT | A | 15 | a0001c0001t0001g0210a0001c0001t0001g0269a0001c0001t0001g0280others(12): Show | 15 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-19798_-177-19 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657858 | ||||||
| chr3:139657906
|
G | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0130others(59): Show | 65 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-178+19799C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657906 | ||||||
| chr3:139657913
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-178+19792C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657913 | ||||||
| chr3:139657967
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-178+19738A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657967 | ||||||
| chr3:139658184
|
G | A | 61 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(58): Show | 63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-178+19521C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658184 | ||||||
| chr3:139658355
|
C | T | 6 | a0001c0001t0001g0127a0001c0001t0002g0053a0001c0002t0002g0040others(3): Show | 6 | HG01496.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-178+19350G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658355 | ||||||
| chr3:139658425
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0003g0177 | 3 | HG00735.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-178+19280A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658425 | ||||||
| chr3:139658433
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(75): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-178+19272G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658433 | ||||||
| chr3:139658479
|
T | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0100others(211): Show | 218 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-178+19226A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658479 | ||||||
| chr3:139658502
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-178+19203G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658502 | ||||||
| chr3:139658564
|
T | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0100others(210): Show | 217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-178+19141A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658564 | ||||||
| chr3:139658661
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-178+19044G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658661 | ||||||
| chr3:139658668
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-178+19037A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658668 | ||||||
| chr3:139658778
|
G | A | 5 | a0001c0001t0001g0200a0001c0001t0001g0287a0001c0001t0001g0288others(2): Show | 5 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-178+18927C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658778 | ||||||
| chr3:139658886
|
TC | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0100others(206): Show | 213 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-178+18818delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658886 | ||||||
| chr3:139658949
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-178+18756C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658949 | ||||||
| chr3:139659002
|
C | T | 2 | a0001c0001t0002g0009a0004c0008t0001g0160 | 2 | HG01099.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-178+18703G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659002 | ||||||
| chr3:139659219
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-178+18486A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659219 | ||||||
| chr3:139659313
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0101others(91): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-178+18392T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659313 | ||||||
| chr3:139659543
|
T | C | 19 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0008others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+18162A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659543 | ||||||
| chr3:139659597
|
TA | T | 17 | a0001c0001t0001g0210a0001c0001t0001g0269a0001c0001t0001g0280others(14): Show | 17 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+18107delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659597 | ||||||
| chr3:139659730
|
C | A | 11 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0191others(8): Show | 11 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+17975G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659730 | ||||||
| chr3:139659760
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-178+17945T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659760 | ||||||
| chr3:139659789
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-178+17916G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659789 | ||||||
| chr3:139660142
|
G | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0101others(91): Show | 96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-178+17563C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660142 | ||||||
| chr3:139660169
|
A | C | 19 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0008others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17536T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660169 | ||||||
| chr3:139660321
|
A | G | 19 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0008others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17384T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660321 | ||||||
| chr3:139660358
|
T | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0127others(78): Show | 83 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.-178+17347A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660358 | ||||||
| chr3:139660463
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-178+17242A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660463 | ||||||
| chr3:139660476
|
A | G | 19 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0008others(16): Show | 19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17229T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660476 | ||||||
| chr3:139660543
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0131a0001c0001t0001g0133others(78): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-178+17162C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660543 | ||||||
| chr3:139660832
|
TA | T | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0100others(210): Show | 217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-178+16872delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660832 | ||||||
| chr3:139660913
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-178+16792T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660913 | ||||||
| chr3:139661006
|
T | G | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0004c0008t0001g0160 | 3 | HG01099.hp2 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-178+16699A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661006 | ||||||
| chr3:139661098
|
C | T | 18 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0010others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-178+16607G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661098 | ||||||
| chr3:139661215
|
A | C | 18 | a0001c0001t0001g0210a0001c0001t0001g0269a0001c0001t0001g0280others(15): Show | 18 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-178+16490T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661215 | ||||||
| chr3:139661255
|
T | A | 1 | a0001c0001t0002g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-178+16450A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661255 | ||||||
| chr3:139661293
|
G | A | 10 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0191others(7): Show | 10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-178+16412C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661293 | ||||||
| chr3:139661305
|
C | G | 18 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0002g0010others(15): Show | 18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-178+16400G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661305 | ||||||
| chr3:139661352
|
G | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0179others(4): Show | 7 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+16353C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661352 | ||||||
| chr3:139661388
|
G | T | 8 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0181others(5): Show | 8 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-178+16317C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661388 | ||||||
| chr3:139661475
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-178+16230A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661475 | ||||||
| chr3:139661631
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0162others(55): Show | 60 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-178+16074G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661631 | ||||||
| chr3:139661924
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0200a0001c0001t0001g0287others(3): Show | 7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+15781C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661924 | ||||||
| chr3:139662374
|
G | T | 1 | a0001c0001t0001g0297 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-178+15331C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662374 | ||||||
| chr3:139662726
|
G | A | 3 | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0029 | 3 | HG00639.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-178+14979C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662726 | ||||||
| chr3:139662983
|
G | A | 8 | a0001c0001t0001g0127a0001c0001t0001g0181a0001c0001t0002g0010others(5): Show | 8 | HG01496.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+14722C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662983 | ||||||
| chr3:139663005
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-178+14700T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663005 | ||||||
| chr3:139663237
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-178+14468A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663237 | ||||||
| chr3:139663380
|
C | T | 3 | a0001c0001t0001g0212a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18946.hp1 NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-178+14325G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663380 | ||||||
| chr3:139663570
|
T | C | 1 | a0001c0001t0001g0291 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-178+14135A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663570 | ||||||
| chr3:139663773
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0194 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-178+13932G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663773 | ||||||
| chr3:139663937
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-178+13768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663937 | ||||||
| chr3:139663966
|
G | GT | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0219others(1): Show | 4 | HG02145.hp2 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+13738dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663966 | ||||||
| chr3:139664349
|
T | A | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+13356A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664349 | ||||||
| chr3:139664416
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0006g0048 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-178+13289G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664416 | ||||||
| chr3:139664976
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG02145.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-178+12729A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664976 | ||||||
| chr3:139665098
|
A | G | 1 | a0001c0004t0001g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-178+12607T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665098 | ||||||
| chr3:139665156
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-178+12549C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665156 | ||||||
| chr3:139665252
|
C | T | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(4): Show | 7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+12453G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665252 | ||||||
| chr3:139665406
|
G | C | 5 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0256others(2): Show | 5 | HG00735.hp1 HG01515.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+12299C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665406 | ||||||
| chr3:139665539
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-178+12166A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665539 | ||||||
| chr3:139665725
|
G | GGA | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 142 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-178+11978_-178+11 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
G | GGAGA | 12 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0176others(9): Show | 12 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11976_-178+11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
G | GGAGAGA | 8 | a0001c0001t0001g0121a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG01175.hp1 HG02145.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+11974_-178+11 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
G | GGAGAGAG others(1): Show |
6 | a0001c0001t0001g0180a0001c0002t0001g0122a0001c0002t0001g0125others(3): Show | 6 | HG02818.hp2 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-178+11972_-178+11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
G | GGAGAGAG others(3): Show |
4 | a0001c0001t0001g0123a0001c0001t0001g0181a0001c0001t0001g0256others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+11970_-178+11 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
GGA | G | 74 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-178+11978_-178+11 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
GGAGA | G | 3 | a0001c0001t0001g0186a0001c0001t0002g0011a0001c0001t0002g0012 | 3 | HG02486.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-178+11976_-178+11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
GGAGAGA | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0184a0001c0001t0002g0094 | 3 | HG03688.hp1 HG04204.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-178+11974_-178+11 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665725
|
GGAGAGAG others(1): Show |
G | 50 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(47): Show | 50 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-178+11972_-178+11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | ||||||
| chr3:139665836
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0273 | 2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-178+11869T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665836 | ||||||
| chr3:139666132
|
C | T | 11 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0275others(8): Show | 11 | HG02071.hp1 HG02165.hp2 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.-178+11573G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666132 | ||||||
| chr3:139666133
|
G | A | 12 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0190others(9): Show | 12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11572C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666133 | ||||||
| chr3:139666186
|
C | A | 12 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0190others(9): Show | 12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11519G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666186 | ||||||
| chr3:139666215
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-178+11490G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666215 | ||||||
| chr3:139666336
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-178+11369G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666336 | ||||||
| chr3:139666415
|
G | A | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0121others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-178+11290C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666415 | ||||||
| chr3:139666444
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | HG02896.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-178+11261T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666444 | ||||||
| chr3:139666554
|
C | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0196a0001c0001t0001g0197others(62): Show | 66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-178+11151G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666554 | ||||||
| chr3:139666591
|
C | T | 22 | a0001c0001t0001g0003a0001c0001t0001g0129a0001c0001t0001g0132others(19): Show | 23 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-178+11114G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666591 | ||||||
| chr3:139666892
|
C | G | 12 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0190others(9): Show | 12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+10813G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666892 | ||||||
| chr3:139666896
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-178+10809C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666896 | ||||||
| chr3:139666901
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-178+10804A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666901 | ||||||
| chr3:139666912
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-178+10793C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666912 | ||||||
| chr3:139667015
|
G | T | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(4): Show | 7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+10690C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667015 | ||||||
| chr3:139667039
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+10666A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667039 | ||||||
| chr3:139667081
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+10624T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667081 | ||||||
| chr3:139667671
|
T | G | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0126others(57): Show | 62 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-178+10034A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667671 | ||||||
| chr3:139667712
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-178+9993T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667712 | ||||||
| chr3:139667746
|
T | A | 9 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0190others(6): Show | 9 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-178+9959A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667746 | ||||||
| chr3:139667873
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-178+9832A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667873 | ||||||
| chr3:139668108
|
C | G | 1 | a0001c0004t0001g0120 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-178+9597G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668108 | ||||||
| chr3:139668357
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+9348T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668357 | ||||||
| chr3:139668441
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-178+9264T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668441 | ||||||
| chr3:139668850
|
A | G | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | HG00280.hp1 HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-178+8855T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668850 | ||||||
| chr3:139669015
|
G | A | 26 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0001others(23): Show | 28 | HG00099.hp2 HG00738.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-178+8690C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669015 | ||||||
| chr3:139669029
|
T | A | 12 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0001g0190others(9): Show | 12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+8676A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669029 | ||||||
| chr3:139669198
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0002g0066 | 2 | HG01243.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-178+8507G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669198 | ||||||
| chr3:139669264
|
G | C | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-178+8441C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669264 | ||||||
| chr3:139669455
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-178+8250G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669455 | ||||||
| chr3:139669476
|
C | CA | 10 | a0001c0001t0001g0203a0001c0001t0001g0261a0001c0001t0001g0263others(7): Show | 10 | HG01255.hp1 NA18966.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-178+8228dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669476 | ||||||
| chr3:139669477
|
AG | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0196a0001c0001t0001g0197others(42): Show | 46 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.-178+8227delC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669477 | ||||||
| chr3:139669478
|
G | A | 17 | a0001c0001t0001g0203a0001c0001t0001g0234a0001c0001t0001g0258others(14): Show | 17 | HG01123.hp2 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-178+8227C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | ||||||
| chr3:139669478
|
G | GA | 67 | a0001c0001t0001g0107a0001c0001t0001g0127a0001c0001t0001g0131others(64): Show | 69 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-178+8226dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | ||||||
| chr3:139669478
|
G | GAA | 11 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(8): Show | 11 | HG01167.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+8225_-178+822 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | ||||||
| chr3:139669478
|
GAAAAAAA | G | 17 | a0001c0001t0001g0200a0001c0001t0001g0210a0001c0001t0001g0275others(14): Show | 17 | HG01192.hp2 HG01256.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+8220_-178+822 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | ||||||
| chr3:139669971
|
C | T | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(4): Show | 7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+7734G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669971 | ||||||
| chr3:139670103
|
G | T | 26 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0001others(23): Show | 28 | HG00099.hp2 HG00738.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-178+7602C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670103 | ||||||
| chr3:139670222
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-178+7483G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670222 | ||||||
| chr3:139670242
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01099.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+7463C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670242 | ||||||
| chr3:139670408
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-178+7297A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670408 | ||||||
| chr3:139670420
|
C | T | 4 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+7285G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670420 | ||||||
| chr3:139670504
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-178+7201T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670504 | ||||||
| chr3:139670511
|
A | G | 2 | a0001c0001t0001g0130a0001c0001t0001g0184 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-178+7194T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670511 | ||||||
| chr3:139670758
|
T | C | 10 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0026others(7): Show | 10 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-178+6947A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670758 | ||||||
| chr3:139670782
|
T | C | 1 | a0001c0001t0001g0311 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-178+6923A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670782 | ||||||
| chr3:139670910
|
A | T | 2 | a0001c0001t0002g0035a0001c0001t0002g0054 | 2 | HG00738.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-178+6795T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670910 | ||||||
| chr3:139671078
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+6627T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671078 | ||||||
| chr3:139671234
|
C | T | 6 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0031others(3): Show | 6 | HG01069.hp2 HG01106.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-178+6471G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671234 | ||||||
| chr3:139671478
|
T | C | 1 | a0001c0003t0002g0091 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-178+6227A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671478 | ||||||
| chr3:139671552
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-178+6153G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671552 | ||||||
| chr3:139671618
|
T | A | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0003c0005t0002g0030 | 3 | HG02965.hp1 NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-178+6087A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | ||||||
| chr3:139671618
|
T | TCA | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0126others(60): Show | 65 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-178+6085_-178+608 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | ||||||
| chr3:139671618
|
T | TCACA | 66 | a0001c0001t0001g0005a0001c0001t0001g0196a0001c0001t0001g0197others(63): Show | 67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-178+6083_-178+608 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | ||||||
| chr3:139671620
|
A | T | 4 | a0001c0001t0001g0129a0001c0001t0002g0010a0001c0004t0001g0120others(1): Show | 4 | HG01175.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+6085T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671620 | ||||||
| chr3:139671657
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+6048G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671657 | ||||||
| chr3:139671971
|
G | A | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-178+5734C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671971 | ||||||
| chr3:139671977
|
G | A | 5 | a0001c0001t0002g0089a0001c0003t0001g0193a0001c0003t0002g0061others(2): Show | 5 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+5728C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671977 | ||||||
| chr3:139671997
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-178+5708A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671997 | ||||||
| chr3:139671997
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-178+5708A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671997 | ||||||
| chr3:139672031
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-178+5674G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672031 | ||||||
| chr3:139672111
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0051a0001c0001t0002g0052 | 4 | HG00099.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+5594A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672111 | ||||||
| chr3:139672114
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-178+5591C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672114 | ||||||
| chr3:139672156
|
C | T | 1 | a0001c0001t0002g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-178+5549G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672156 | ||||||
| chr3:139672219
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-178+5486T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672219 | ||||||
| chr3:139672290
|
G | T | 49 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(46): Show | 49 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-178+5415C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672290 | ||||||
| chr3:139672326
|
T | C | 94 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0204others(91): Show | 96 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-178+5379A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672326 | ||||||
| chr3:139672332
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-178+5373G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672332 | ||||||
| chr3:139672388
|
T | C | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-178+5317A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672388 | ||||||
| chr3:139672619
|
T | TG | 5 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0003t0002g0061others(2): Show | 5 | HG01123.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+5085dupC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672619 | ||||||
| chr3:139672643
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-178+5062T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672643 | ||||||
| chr3:139673105
|
C | T | 1 | a0004c0008t0001g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-178+4600G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673105 | ||||||
| chr3:139673162
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+4543C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673162 | ||||||
| chr3:139673239
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0020 | 3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+4466A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673239 | ||||||
| chr3:139673264
|
G | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0020 | 3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+4441C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673264 | ||||||
| chr3:139673304
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-178+4401G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673304 | ||||||
| chr3:139673356
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-178+4349A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673356 | ||||||
| chr3:139673367
|
T | G | 4 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0312others(1): Show | 4 | NA18941.hp1 NA18969.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+4338A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673367 | ||||||
| chr3:139673473
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0092 | 3 | NA18942.hp2 NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-178+4232C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673473 | ||||||
| chr3:139673526
|
T | C | 235 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0121others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-178+4179A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673526 | ||||||
| chr3:139673563
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG02015.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.-178+4142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673563 | ||||||
| chr3:139673585
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-178+4120G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673585 | ||||||
| chr3:139673693
|
A | G | 88 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0001others(85): Show | 90 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.-178+4012T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673693 | ||||||
| chr3:139673816
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-178+3889C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673816 | ||||||
| chr3:139673904
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG01167.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+3801G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673904 | ||||||
| chr3:139673998
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0020 | 3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+3707G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673998 | ||||||
| chr3:139673999
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-178+3706C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673999 | ||||||
| chr3:139674078
|
G | T | 1 | a0001c0003t0002g0061 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-178+3627C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674078 | ||||||
| chr3:139674079
|
A | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+3626T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674079 | ||||||
| chr3:139674080
|
T | C | 220 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0126others(217): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-178+3625A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674080 | ||||||
| chr3:139674109
|
C | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0126others(208): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-178+3596G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674109 | ||||||
| chr3:139674278
|
G | A | 1 | a0003c0005t0002g0030 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-178+3427C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674278 | ||||||
| chr3:139674289
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-178+3416C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674289 | ||||||
| chr3:139674379
|
C | T | 12 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(9): Show | 12 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+3326G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674379 | ||||||
| chr3:139674523
|
G | C | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0018others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-178+3182C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674523 | ||||||
| chr3:139674626
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-178+3079G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674626 | ||||||
| chr3:139674640
|
T | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+3065A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674640 | ||||||
| chr3:139674769
|
G | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(1): Show | 4 | HG01069.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+2936C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674769 | ||||||
| chr3:139674800
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-178+2905A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674800 | ||||||
| chr3:139674871
|
T | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+2834A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674871 | ||||||
| chr3:139674991
|
T | C | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(83): Show | 88 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-178+2714A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674991 | ||||||
| chr3:139674998
|
G | C | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(4): Show | 7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+2707C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674998 | ||||||
| chr3:139675135
|
T | TAC | 47 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(44): Show | 47 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-178+2568_-178+256 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(3): Show |
75 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0001g0199others(72): Show | 75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-178+2560_-178+256 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(5): Show |
45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0186others(42): Show | 47 | HG00621.hp1 HG00621.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.-178+2558_-178+256 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(7): Show |
4 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(1): Show | 4 | HG00423.hp1 HG02896.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+2556_-178+256 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(9): Show |
12 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(9): Show | 12 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(15): Show |
2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG01169.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(17): Show |
41 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(38): Show | 41 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(19): Show |
26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0035others(23): Show | 28 | HG00099.hp2 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(30): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(9): Show |
2 | a0001c0001t0002g0008a0001c0001t0002g0020 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+2554_-178+256 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
T | TACACACA others(11): Show |
2 | a0001c0001t0001g0316a0001c0001t0002g0009 | 2 | HG01099.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-178+2552_-178+256 others(22): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675135
|
TAC | T | 15 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0001t0002g0010others(12): Show | 15 | HG01081.hp1 HG01175.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+2568_-178+256 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | ||||||
| chr3:139675197
|
G | T | 12 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0025others(9): Show | 12 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+2508C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675197 | ||||||
| chr3:139675311
|
G | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+2394C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675311 | ||||||
| chr3:139675362
|
A | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+2343T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675362 | ||||||
| chr3:139675393
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-178+2312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675393 | ||||||
| chr3:139675399
|
CAGTT | C | 46 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0021others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-178+2302_-178+230 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675399 | ||||||
| chr3:139675679
|
C | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0002g0021others(1): Show | 4 | HG02145.hp2 HG02602.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+2026G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675679 | ||||||
| chr3:139675729
|
T | C | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+1976A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675729 | ||||||
| chr3:139675743
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-178+1962C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675743 | ||||||
| chr3:139675869
|
G | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+1836C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675869 | ||||||
| chr3:139675937
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-178+1768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675937 | ||||||
| chr3:139675946
|
A | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+1759T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675946 | ||||||
| chr3:139676207
|
T | C | 1 | a0001c0001t0001g0317 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-178+1498A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676207 | ||||||
| chr3:139676419
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+1286T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676419 | ||||||
| chr3:139676426
|
A | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-178+1279T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676426 | ||||||
| chr3:139676439
|
A | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(82): Show | 87 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-178+1266T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676439 | ||||||
| chr3:139676456
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-178+1249T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676456 | ||||||
| chr3:139676505
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-178+1200G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676505 | ||||||
| chr3:139676597
|
G | C | 7 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(4): Show | 7 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-178+1108C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676597 | ||||||
| chr3:139676632
|
G | C | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-178+1073C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676632 | ||||||
| chr3:139676737
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-178+968T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676737 | ||||||
| chr3:139676849
|
A | G | 22 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(19): Show | 22 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-178+856T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676849 | ||||||
| chr3:139676943
|
A | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-178+762T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676943 | ||||||
| chr3:139676958
|
T | C | 81 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0008others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-178+747A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676958 | ||||||
| chr3:139677172
|
T | G | 1 | a0001c0002t0001g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-178+533A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677172 | ||||||
| chr3:139677320
|
T | C | 235 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(232): Show | 238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-178+385A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677320 | ||||||
| chr3:139677330
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-178+375G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677330 | ||||||
| chr3:139677547
|
C | G | 7 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(4): Show | 7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+158G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677547 | ||||||
| chr3:139677561
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01099.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+144G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677561 | ||||||
| chr3:139677608
|
C | T | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-178+97G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677608 | ||||||
| chr3:139677620
|
T | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0196others(124): Show | 129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-178+85A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677620 |