Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64802 |
| ensemblid | ENSG00000173614.14 |
| hgncid | 17877 |
| symbol | NMNAT1 |
| name | nicotinamide nucleotide adenylyltransferase 1 |
| refseq_nuc | NM_022787.4 |
| refseq_prot | NP_073624.2 |
| ensembl_nuc | ENST00000377205.6 |
| ensembl_prot | ENSP00000366410.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 9943475 |
| end | 9985498 |
| strand | + |
| ver | v1.2 |
| region | chr1:9943475-9985498 |
| region5000 | chr1:9938475-9990498 |
| regionname0 | NMNAT1_chr1_9943475_9985498 |
| regionname5000 | NMNAT1_chr1_9938475_9990498 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 279 | 308 | 87 | 52 | 117 | 6 | 44 | 90 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | MENSE others(274): Show |
chr1 | 9938475 | 9990498 |
| a0002 | 0/0 | 279 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | MENSE others(274): Show |
chr1 | 9938475 | 9990498 |
| a0003 | 0/0 | 279 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | MENSE others(274): Show |
chr1 | 9938475 | 9990498 |
| a0004 | 0/0 | 279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | MENSE others(274): Show |
chr1 | 9938475 | 9990498 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 837 | 308 | 87 | 52 | 117 | 6 | 44 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | ATGGA others(832): Show |
chr1 | 9938475 | 9990498 | ||
| a0002c0002 | 0/0 | 837 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | ATGGA others(832): Show |
chr1 | 9938475 | 9990498 | ||
| a0003c0004 | 0/0 | 837 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | ATGGA others(832): Show |
chr1 | 9938475 | 9990498 | ||
| a0004c0003 | 0/0 | 837 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | ATGGA others(832): Show |
chr1 | 9938475 | 9990498 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3734 | 73 | 5 | 20 | 26 | 4 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0002 | 0/0 | 3735 | 74 | 22 | 7 | 27 | 1 | 17 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0003 | 0/0 | 3734 | 52 | 8 | 10 | 30 | 0 | 4 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0004 | 1/0 | 3734 | 26 | 22 | 2 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0005 | 0/0 | 3734 | 20 | 0 | 1 | 19 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0006 | 0/0 | 3733 | 17 | 0 | 6 | 10 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3728): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0007 | 0/0 | 3734 | 7 | 6 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0008 | 0/0 | 3734 | 6 | 6 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0009 | 0/0 | 3735 | 5 | 5 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0010 | 0/0 | 3734 | 5 | 1 | 3 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0011 | 0/0 | 3734 | 3 | 0 | 0 | 0 | 0 | 3 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0012 | 0/0 | 3735 | 3 | 3 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0013 | 0/0 | 3734 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0014 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0015 | 0/0 | 3734 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0016 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0017 | 0/0 | 3735 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0018 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0019 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0020 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3730): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0022 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0023 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0024 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0025 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0026 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0001c0001t0027 | 0/0 | 3752 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3747): Show |
chr1 | 9938475 | 9990498 |
| a0002c0002t0003 | 0/0 | 3734 | 4 | 0 | 0 | 4 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0003c0004t0001 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| a0004c0003t0021 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | GATCT others(3729): Show |
chr1 | 9938475 | 9990498 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0001 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0011 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0010g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0010g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0012g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0012g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0015g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0015g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0016g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0017g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0019g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0020g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0022g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0024g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0025g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0026g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0001c0001t0027g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0002c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| a0004c0003t0021g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0022 | EUR | GBR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | GBR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | FIN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0279 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00558 | hp1 | a0003 | c0004 | t0001 | g0236 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0255 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | CHS | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0086 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0168 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01258 | hp1 | a0001 | c0001 | t0010 | g0169 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01361 | hp2 | a0001 | c0001 | t0025 | g0198 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0287 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01433 | hp2 | a0001 | c0001 | t0020 | g0027 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0084 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0172 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0274 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0063 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0275 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0283 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0267 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0087 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0276 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CDX | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CDX | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0174 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0286 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02451 | hp2 | a0001 | c0001 | t0027 | g0016 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02572 | hp1 | a0001 | c0001 | t0024 | g0089 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0083 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02723 | hp2 | a0001 | c0001 | t0022 | g0065 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02922 | hp2 | a0001 | c0001 | t0012 | g0020 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0223 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0017 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0290 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03491 | hp2 | a0001 | c0001 | t0011 | g0224 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0225 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0021 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0288 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04184 | hp2 | a0001 | c0001 | t0017 | g0212 | SAS | BEB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04228 | hp1 | a0001 | c0001 | t0016 | g0240 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18906 | hp2 | a0001 | c0001 | t0026 | g0028 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18951 | hp1 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0253 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18967 | hp2 | a0001 | c0001 | t0013 | g0046 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18972 | hp2 | a0001 | c0001 | t0018 | g0070 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0270 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18989 | hp2 | a0002 | c0002 | t0003 | g0036 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0040 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0243 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19068 | hp1 | a0001 | c0001 | t0013 | g0043 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19072 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0018 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ASW | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | TSI | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | GIH | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02109 | hp1 | a0004 | c0003 | t0021 | g0015 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0268 | AFR | USA | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0187 | REF | REF | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0011 | REF | REF | NMNAT1_chr1_9938475_9990498 | NMNAT1 | chr1 | 9938475 | 9990498 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9972091 | G | T | 1 | a0003 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.18G>T | p.Lys6Asn | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/5 | 115/3734 | 18/840 | 6/279 | chr1 | 9972091 | |||
| chr1:9972096 | A | C | 1 | a0004 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.23A>C | p.Glu8Ala | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/5 | 120/3734 | 23/840 | 8/279 | chr1 | 9972096 | |||
| chr1:9982625 | G | A | 1 | a0002 | 4 | NA18983.hp2 NA18989.hp2 NA18992.hp2 others(1): Show |
missense_variant | MODERATE | c.764G>A | p.Ser255Asn | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 861/3734 | 764/840 | 255/279 | chr1 | 9982625 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9943481 | C | T | 1 | a0001c0001t0027 | 1 | HG02451.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/5 | chr1 | 9943481 | |||||||
| chr1:9982717 | A | G | 1 | a0001c0001t0026 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 16 | chr1 | 9982717 | ||||||
| chr1:9982846 | G | A | 1 | a0001c0001t0013 | 2 | NA18967.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*145G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 145 | chr1 | 9982846 | ||||||
| chr1:9982903 | C | T | 1 | a0001c0001t0025 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 202 | chr1 | 9982903 | ||||||
| chr1:9983053 | C | T | 2 | a0001c0001t0007 a0001c0001t0024 |
8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 352 | chr1 | 9983053 | ||||||
| chr1:9983084 | G | A | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(5): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*383G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 383 | chr1 | 9983084 | ||||||
| chr1:9983104 | C | CA | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0012 others(2): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*418dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 419 | INFO_REALIGN_3_PRIME | chr1 | 9983104 | |||||
| chr1:9983104 | CA | C | 2 | a0001c0001t0006 a0001c0001t0008 |
23 | HG00408.hp1 HG00558.hp2 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*418delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 418 | INFO_REALIGN_3_PRIME | chr1 | 9983104 | |||||
| chr1:9983226 | A | G | 1 | a0001c0001t0009 | 5 | HG02257.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 525 | chr1 | 9983226 | ||||||
| chr1:9983246 | T | G | 1 | a0001c0001t0016 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 545 | chr1 | 9983246 | ||||||
| chr1:9983308 | T | G | 1 | a0001c0001t0015 | 2 | HG01884.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*607T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 607 | chr1 | 9983308 | ||||||
| chr1:9983358 | G | A | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*657G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 657 | chr1 | 9983358 | ||||||
| chr1:9983400 | A | G | 9 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0018 others(6): Show |
64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 699 | chr1 | 9983400 | ||||||
| chr1:9983635 | G | A | 1 | a0001c0001t0024 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 934 | chr1 | 9983635 | ||||||
| chr1:9983655 | C | CA | 3 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0020 |
8 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*968dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 969 | INFO_REALIGN_3_PRIME | chr1 | 9983655 | |||||
| chr1:9983764 | G | C | 1 | a0001c0001t0010 | 5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1063 | chr1 | 9983764 | ||||||
| chr1:9983764 | G | T | 1 | a0001c0001t0005 | 20 | HG00597.hp1 HG00597.hp2 HG01943.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1063 | chr1 | 9983764 | ||||||
| chr1:9983782 | G | T | 2 | a0001c0001t0010 a0001c0001t0019 |
6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1081 | chr1 | 9983782 | ||||||
| chr1:9983847 | C | T | 1 | a0001c0001t0019 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1146C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1146 | chr1 | 9983847 | ||||||
| chr1:9984204 | T | C | 1 | a0001c0001t0014 | 2 | HG03225.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1503T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1503 | chr1 | 9984204 | ||||||
| chr1:9984390 | A | AAGAACAA others(11): Show |
1 | a0001c0001t0027 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1701_*1718dupTGTA others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 1719 | INFO_REALIGN_3_PRIME | chr1 | 9984390 | |||||
| chr1:9985094 | C | G | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*2393C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2393 | chr1 | 9985094 | ||||||
| chr1:9985160 | C | T | 1 | a0001c0001t0023 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2459 | chr1 | 9985160 | ||||||
| chr1:9985223 | A | T | 1 | a0001c0001t0022 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2522 | chr1 | 9985223 | ||||||
| chr1:9985232 | G | A | 1 | a0001c0001t0011 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2531G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2531 | chr1 | 9985232 | ||||||
| chr1:9985240 | A | T | 1 | a0004c0003t0021 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2539A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 5/5 | 2539 | chr1 | 9985240 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:9943750 | C | A | 2 | a0001c0001t0027g0016 a0004c0003t0021g0015 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-57+235C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9943750 | |||||||
| chr1:9943897 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+382C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9943897 | |||||||
| chr1:9944014 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+499G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944014 | |||||||
| chr1:9944026 | A | G | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+511A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944026 | |||||||
| chr1:9944030 | G | A | 1 | a0001c0001t0010g0022 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-57+515G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944030 | |||||||
| chr1:9944247 | C | T | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+732C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944247 | |||||||
| chr1:9944285 | C | T | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+770C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944285 | |||||||
| chr1:9944289 | C | T | 17 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0274 others(14): Show |
17 | HG00408.hp1 HG00558.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+774C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944289 | |||||||
| chr1:9944292 | G | A | 57 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+777G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944292 | |||||||
| chr1:9944293 | G | T | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-57+778G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944293 | |||||||
| chr1:9944550 | G | A | 57 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+1035G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944550 | |||||||
| chr1:9944816 | C | CAGAGTTA others(9): Show |
1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+1302_-57+1317d others(18): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9944816 | ||||||
| chr1:9944824 | C | T | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57+1309C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944824 | |||||||
| chr1:9944979 | A | C | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+1464A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9944979 | |||||||
| chr1:9945048 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-57+1533A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945048 | |||||||
| chr1:9945238 | AC | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+1724delC | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945238 | |||||||
| chr1:9945817 | G | A | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+2302G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945817 | |||||||
| chr1:9945936 | T | C | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+2421T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9945936 | |||||||
| chr1:9946013 | C | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+2498C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946013 | |||||||
| chr1:9946320 | C | T | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-57+2805C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946320 | |||||||
| chr1:9946342 | T | G | 1 | a0001c0001t0006g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57+2827T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946342 | |||||||
| chr1:9946434 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2919A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946434 | |||||||
| chr1:9946435 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2920G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946435 | |||||||
| chr1:9946514 | T | A | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+2999T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946514 | |||||||
| chr1:9946705 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+3190A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946705 | |||||||
| chr1:9946724 | A | T | 2 | a0001c0001t0005g0269 a0001c0001t0005g0270 |
2 | NA18974.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-57+3209A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9946724 | |||||||
| chr1:9947291 | G | A | 16 | a0001c0001t0004g0006 a0001c0001t0004g0080 a0001c0001t0004g0081 others(13): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+3776G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947291 | |||||||
| chr1:9947376 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-57+3861C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947376 | |||||||
| chr1:9947470 | A | T | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+3955A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947470 | |||||||
| chr1:9947638 | T | G | 4 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(1): Show |
4 | HG02717.hp1 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+4123T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947638 | |||||||
| chr1:9947704 | C | T | 1 | a0001c0001t0006g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-57+4189C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947704 | |||||||
| chr1:9947765 | T | G | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-57+4250T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947765 | |||||||
| chr1:9947789 | G | T | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | NA18970.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-57+4274G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947789 | |||||||
| chr1:9947955 | G | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4440G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9947955 | |||||||
| chr1:9948098 | A | T | 1 | a0001c0001t0002g0075 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-57+4583A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948098 | |||||||
| chr1:9948133 | G | A | 57 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+4618G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948133 | |||||||
| chr1:9948163 | G | A | 119 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(116): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-57+4648G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948163 | |||||||
| chr1:9948242 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-57+4727C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948242 | |||||||
| chr1:9948307 | G | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4792G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948307 | |||||||
| chr1:9948372 | C | T | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-57+4857C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948372 | |||||||
| chr1:9948468 | T | C | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+4953T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948468 | |||||||
| chr1:9948505 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+4990C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948505 | |||||||
| chr1:9948560 | C | T | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+5045C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948560 | |||||||
| chr1:9948605 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-57+5090T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948605 | |||||||
| chr1:9948651 | A | AT | 18 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0003g0003 others(15): Show |
23 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+5151dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9948651 | ||||||
| chr1:9948710 | C | G | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+5195C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948710 | |||||||
| chr1:9948710 | C | T | 1 | a0001c0001t0003g0073 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-57+5195C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948710 | |||||||
| chr1:9948802 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-57+5287A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948802 | |||||||
| chr1:9948868 | G | A | 6 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+5353G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948868 | |||||||
| chr1:9948947 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | NA18977.hp1 NA18989.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.-57+5432C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9948947 | |||||||
| chr1:9949056 | C | T | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-57+5541C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949056 | |||||||
| chr1:9949080 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57+5565A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949080 | |||||||
| chr1:9949150 | A | G | 1 | a0001c0001t0004g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+5635A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949150 | |||||||
| chr1:9949160 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-57+5645C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949160 | |||||||
| chr1:9949161 | G | A | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+5646G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949161 | |||||||
| chr1:9949294 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57+5779C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949294 | |||||||
| chr1:9949349 | A | G | 3 | a0001c0001t0003g0058 a0001c0001t0003g0059 a0001c0001t0003g0060 |
3 | HG00408.hp2 HG02165.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-57+5834A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949349 | |||||||
| chr1:9949410 | C | CT | 40 | a0001c0001t0002g0158 a0001c0001t0002g0164 a0001c0001t0003g0002 others(37): Show |
42 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+5912dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | ||||||
| chr1:9949410 | C | CTTT | 111 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(108): Show |
113 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-57+5910_-57+5912d others(5): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | ||||||
| chr1:9949410 | C | CTTTT | 8 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0005g0255 others(5): Show |
8 | HG00597.hp1 HG00597.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+5909_-57+5912d others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949410 | ||||||
| chr1:9949534 | C | T | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+6019C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949534 | |||||||
| chr1:9949535 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-57+6020G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949535 | |||||||
| chr1:9949580 | T | TTG | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-57+6073_-57+6074d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949580 | ||||||
| chr1:9949588 | G | GTA | 57 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+6085_-57+6086d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9949588 | ||||||
| chr1:9949804 | A | G | 2 | a0001c0001t0005g0254 a0001c0001t0005g0260 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+6289A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949804 | |||||||
| chr1:9949867 | T | C | 55 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(52): Show |
63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-57+6352T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949867 | |||||||
| chr1:9949956 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-57+6441A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9949956 | |||||||
| chr1:9950286 | T | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+6771T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950286 | |||||||
| chr1:9950338 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-57+6823G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950338 | |||||||
| chr1:9950554 | A | G | 1 | a0001c0001t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+7039A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950554 | |||||||
| chr1:9950784 | C | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7269C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950784 | |||||||
| chr1:9950827 | A | G | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+7312A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950827 | |||||||
| chr1:9950897 | T | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0023 a0001c0001t0003g0037 others(25): Show |
30 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+7382T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950897 | |||||||
| chr1:9950920 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-57+7405C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9950920 | |||||||
| chr1:9951013 | C | A | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-57+7498C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951013 | |||||||
| chr1:9951047 | C | T | 8 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+7532C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951047 | |||||||
| chr1:9951054 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-57+7539A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951054 | |||||||
| chr1:9951088 | CA | C | 19 | a0001c0001t0001g0175 a0001c0001t0001g0248 a0001c0001t0001g0249 others(16): Show |
19 | HG01884.hp2 HG02165.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.-57+7589delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9951088 | ||||||
| chr1:9951107 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 |
3 | HG02895.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-57+7592G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951107 | |||||||
| chr1:9951108 | G | A | 3 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 |
3 | HG02895.hp2 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-57+7593G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951108 | |||||||
| chr1:9951462 | T | G | 73 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(70): Show |
83 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+7947T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951462 | |||||||
| chr1:9951465 | G | T | 29 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0093 others(26): Show |
30 | HG01167.hp2 HG01943.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+7950G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951465 | |||||||
| chr1:9951476 | T | C | 2 | a0001c0001t0002g0163 a0001c0001t0002g0164 |
2 | NA18970.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.-57+7961T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951476 | |||||||
| chr1:9951477 | G | GTTGT | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57+7973_-57+7976d others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9951477 | ||||||
| chr1:9951621 | C | T | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+8106C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951621 | |||||||
| chr1:9951713 | G | T | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+8198G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951713 | |||||||
| chr1:9951912 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-57+8397A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9951912 | |||||||
| chr1:9952088 | G | A | 57 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(54): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-57+8573G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952088 | |||||||
| chr1:9952134 | T | TA | 29 | a0001c0001t0002g0075 a0001c0001t0003g0002 a0001c0001t0003g0023 others(26): Show |
31 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-57+8628dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9952134 | ||||||
| chr1:9952149 | A | T | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8634A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952149 | |||||||
| chr1:9952207 | C | T | 2 | a0001c0001t0005g0254 a0001c0001t0005g0260 |
2 | NA18970.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-57+8692C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952207 | |||||||
| chr1:9952253 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+8738G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952253 | |||||||
| chr1:9952582 | G | T | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+9067G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952582 | |||||||
| chr1:9952819 | G | A | 1 | a0001c0001t0005g0243 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-57+9304G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952819 | |||||||
| chr1:9952834 | C | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0128 a0001c0001t0002g0129 others(4): Show |
8 | HG02698.hp2 HG03490.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+9319C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952834 | |||||||
| chr1:9952860 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-57+9345C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952860 | |||||||
| chr1:9952956 | A | C | 68 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(65): Show |
76 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-57+9441A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9952956 | |||||||
| chr1:9953003 | C | T | 2 | a0001c0001t0015g0083 a0001c0001t0015g0084 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-57+9488C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953003 | |||||||
| chr1:9953020 | G | A | 2 | a0001c0001t0010g0168 a0001c0001t0010g0169 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-57+9505G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953020 | |||||||
| chr1:9953137 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-57+9622C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953137 | |||||||
| chr1:9953278 | C | CT | 23 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 others(20): Show |
23 | HG00423.hp1 HG00597.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-57+9780dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953278 | ||||||
| chr1:9953278 | CT | C | 36 | a0001c0001t0001g0176 a0001c0001t0002g0009 a0001c0001t0002g0010 others(33): Show |
40 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9780delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953278 | ||||||
| chr1:9953327 | A | G | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-57+9812A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953327 | |||||||
| chr1:9953448 | G | GT | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(119): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-57+9944dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953448 | ||||||
| chr1:9953448 | G | GTT | 7 | a0001c0001t0005g0270 a0001c0001t0006g0283 a0001c0001t0008g0170 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+9943_-57+9944d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953448 | ||||||
| chr1:9953509 | C | T | 1 | a0003c0004t0001g0236 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-57+9994C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953509 | |||||||
| chr1:9953533 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-57+10018C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953533 | |||||||
| chr1:9953667 | G | A | 5 | a0001c0001t0005g0244 a0001c0001t0005g0245 a0001c0001t0005g0253 others(2): Show |
5 | NA18951.hp2 NA18959.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+10152G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9953667 | |||||||
| chr1:9953797 | C | CT | 19 | a0001c0001t0002g0075 a0001c0001t0002g0091 a0001c0001t0002g0103 others(16): Show |
19 | HG00438.hp2 HG01981.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+10308dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | ||||||
| chr1:9953797 | CT | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0234 a0001c0001t0001g0235 others(17): Show |
21 | HG00099.hp1 HG00597.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-57+10308delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | ||||||
| chr1:9953797 | CTT | C | 155 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0175 others(152): Show |
164 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-57+10307_-57+1030 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | ||||||
| chr1:9953797 | CTTT | C | 6 | a0001c0001t0001g0177 a0001c0001t0003g0037 a0001c0001t0003g0055 others(3): Show |
6 | HG00423.hp1 HG00558.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10306_-57+1030 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | ||||||
| chr1:9953797 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-57+10299_-57+1030 others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9953797 | ||||||
| chr1:9954009 | T | G | 1 | a0001c0001t0006g0272 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-57+10494T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954009 | |||||||
| chr1:9954025 | T | G | 1 | a0001c0001t0005g0178 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-57+10510T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954025 | |||||||
| chr1:9954115 | C | G | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+10600C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954115 | |||||||
| chr1:9954121 | A | G | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+10606A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954121 | |||||||
| chr1:9954283 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-57+10768C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954283 | |||||||
| chr1:9954328 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-57+10813A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954328 | |||||||
| chr1:9954376 | ACTT | A | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+10867_-57+1086 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9954376 | ||||||
| chr1:9954489 | A | G | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+10974A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954489 | |||||||
| chr1:9954620 | C | T | 27 | a0001c0001t0002g0009 a0001c0001t0002g0095 a0001c0001t0002g0096 others(24): Show |
30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+11105C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954620 | |||||||
| chr1:9954789 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57+11274C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954789 | |||||||
| chr1:9954799 | C | T | 2 | a0001c0001t0027g0016 a0004c0003t0021g0015 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-57+11284C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954799 | |||||||
| chr1:9954802 | G | A | 6 | a0001c0001t0003g0054 a0001c0001t0010g0022 a0001c0001t0010g0168 others(3): Show |
6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+11287G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9954802 | |||||||
| chr1:9954929 | CA | C | 114 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(111): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-57+11428delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9954929 | ||||||
| chr1:9955129 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+11614G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955129 | |||||||
| chr1:9955369 | A | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0023 a0001c0001t0003g0037 others(25): Show |
30 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-57+11854A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955369 | |||||||
| chr1:9955403 | C | CA | 6 | a0001c0001t0002g0075 a0001c0001t0002g0127 a0001c0001t0002g0167 others(3): Show |
6 | HG01981.hp2 HG02109.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+11907dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | ||||||
| chr1:9955403 | C | CAA | 71 | a0001c0001t0001g0030 a0001c0001t0001g0229 a0001c0001t0001g0230 others(68): Show |
79 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.-57+11906_-57+1190 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | ||||||
| chr1:9955403 | C | CAAA | 95 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-57+11905_-57+1190 others(7): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | ||||||
| chr1:9955403 | C | CAAAA | 18 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(15): Show |
18 | HG00597.hp2 HG01123.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+11904_-57+1190 others(8): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9955403 | ||||||
| chr1:9955418 | A | C | 1 | a0001c0001t0004g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-57+11903A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955418 | |||||||
| chr1:9955474 | G | A | 8 | a0001c0001t0007g0076 a0001c0001t0007g0077 a0001c0001t0007g0078 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+11959G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955474 | |||||||
| chr1:9955504 | C | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0033 others(13): Show |
21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+11989C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955504 | |||||||
| chr1:9955640 | C | T | 63 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(60): Show |
71 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+12125C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955640 | |||||||
| chr1:9955765 | G | A | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12250G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9955765 | |||||||
| chr1:9956104 | A | G | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12589A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956104 | |||||||
| chr1:9956170 | C | CT | 7 | a0001c0001t0003g0051 a0001c0001t0005g0242 a0001c0001t0008g0170 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+12672dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956170 | ||||||
| chr1:9956172 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57+12657T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956172 | |||||||
| chr1:9956175 | T | C | 1 | a0001c0001t0004g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+12660T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956175 | |||||||
| chr1:9956232 | C | T | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+12717C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956232 | |||||||
| chr1:9956236 | C | G | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+12721C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956236 | |||||||
| chr1:9956277 | C | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0176 a0001c0001t0001g0179 others(10): Show |
14 | HG00099.hp2 HG00639.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+12762C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956277 | |||||||
| chr1:9956420 | C | CT | 60 | a0001c0001t0001g0030 a0001c0001t0001g0179 a0001c0001t0001g0232 others(57): Show |
68 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-57+12924dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956420 | ||||||
| chr1:9956420 | CT | C | 90 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0196 others(87): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-57+12924delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956420 | ||||||
| chr1:9956510 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-57+12995C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956510 | |||||||
| chr1:9956707 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-57+13192G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956707 | |||||||
| chr1:9956731 | C | CT | 15 | a0001c0001t0001g0176 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
17 | HG00099.hp2 HG00597.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-57+13234dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956731 | ||||||
| chr1:9956731 | C | CTT | 6 | a0001c0001t0001g0186 a0001c0001t0010g0022 a0001c0001t0010g0168 others(3): Show |
6 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+13233_-57+1323 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9956731 | ||||||
| chr1:9956835 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-57+13320G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956835 | |||||||
| chr1:9956845 | C | T | 1 | a0001c0001t0003g0056 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-57+13330C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956845 | |||||||
| chr1:9956871 | G | A | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-57+13356G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956871 | |||||||
| chr1:9956928 | C | T | 1 | a0001c0001t0005g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57+13413C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956928 | |||||||
| chr1:9956976 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-57+13461C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9956976 | |||||||
| chr1:9957028 | C | T | 2 | a0001c0001t0015g0083 a0001c0001t0015g0084 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-57+13513C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957028 | |||||||
| chr1:9957059 | C | T | 1 | a0001c0001t0005g0228 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-57+13544C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957059 | |||||||
| chr1:9957161 | C | A | 1 | a0001c0001t0008g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-57+13646C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957161 | |||||||
| chr1:9957217 | C | T | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+13702C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957217 | |||||||
| chr1:9957359 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-57+13844C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957359 | |||||||
| chr1:9957469 | G | A | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-57+13954G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957469 | |||||||
| chr1:9957591 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-57+14076C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957591 | |||||||
| chr1:9957828 | C | G | 1 | a0001c0001t0002g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-14190C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957828 | |||||||
| chr1:9957836 | G | A | 1 | a0001c0001t0004g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-56-14182G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957836 | |||||||
| chr1:9957933 | C | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-14085C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9957933 | |||||||
| chr1:9958144 | A | G | 5 | a0001c0001t0008g0170 a0001c0001t0008g0171 a0001c0001t0008g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-13874A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958144 | |||||||
| chr1:9958443 | G | GT | 7 | a0001c0001t0001g0227 a0001c0001t0003g0037 a0001c0001t0003g0039 others(4): Show |
7 | HG00544.hp1 HG01192.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-13561dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9958443 | ||||||
| chr1:9958443 | GT | G | 8 | a0001c0001t0001g0179 a0001c0001t0003g0041 a0001c0001t0006g0285 others(5): Show |
8 | HG02135.hp1 HG02922.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-13561delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9958443 | ||||||
| chr1:9958448 | T | G | 43 | a0001c0001t0001g0200 a0001c0001t0002g0001 a0001c0001t0002g0075 others(40): Show |
48 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.-56-13570T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958448 | |||||||
| chr1:9958453 | T | G | 2 | a0001c0001t0002g0116 a0001c0001t0019g0290 |
2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-13565T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958453 | |||||||
| chr1:9958483 | A | C | 87 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-13535A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958483 | |||||||
| chr1:9958502 | T | C | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-13516T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958502 | |||||||
| chr1:9958591 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-56-13427C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958591 | |||||||
| chr1:9958655 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-56-13363G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958655 | |||||||
| chr1:9958685 | A | G | 283 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(280): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.-56-13333A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9958685 | |||||||
| chr1:9959071 | T | C | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-12947T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959071 | |||||||
| chr1:9959201 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-56-12817A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959201 | |||||||
| chr1:9959296 | C | T | 3 | a0001c0001t0011g0223 a0001c0001t0011g0224 a0001c0001t0011g0225 |
3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-56-12722C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959296 | |||||||
| chr1:9959297 | G | T | 1 | a0001c0001t0002g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-56-12721G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959297 | |||||||
| chr1:9959320 | T | G | 9 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0093 others(6): Show |
10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-12698T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959320 | |||||||
| chr1:9959327 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-56-12691G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959327 | |||||||
| chr1:9959373 | GAAAAAA | G | 14 | a0001c0001t0002g0105 a0001c0001t0002g0127 a0001c0001t0002g0128 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-12625_-56-1262 others(10): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | ||||||
| chr1:9959373 | GAAAAAAA | G | 253 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(250): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-56-12626_-56-1262 others(11): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | ||||||
| chr1:9959373 | GAAAAAAA others(1): Show |
G | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0094 others(5): Show |
8 | HG02004.hp2 HG02451.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-12627_-56-1262 others(12): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9959373 | ||||||
| chr1:9959421 | G | A | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-12597G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959421 | |||||||
| chr1:9959534 | A | T | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-12484A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959534 | |||||||
| chr1:9959639 | C | T | 3 | a0001c0001t0009g0007 a0001c0001t0009g0008 a0001c0001t0009g0139 |
5 | HG02257.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-12379C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959639 | |||||||
| chr1:9959876 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-56-12142T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9959876 | |||||||
| chr1:9960288 | AAAAAACA others(5): Show |
A | 55 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(52): Show |
63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-11718_-56-1170 others(16): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9960288 | ||||||
| chr1:9960295 | AAAAACAA others(4): Show |
A | 1 | a0001c0001t0003g0037 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-56-11718_-56-1170 others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9960295 | ||||||
| chr1:9960836 | T | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-11182T>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960836 | |||||||
| chr1:9960844 | G | A | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-11174G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960844 | |||||||
| chr1:9960881 | G | A | 2 | a0001c0001t0004g0085 a0001c0001t0004g0090 |
2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-56-11137G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9960881 | |||||||
| chr1:9961083 | G | C | 1 | a0001c0001t0004g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-56-10935G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961083 | |||||||
| chr1:9961332 | CTT | C | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-10685_-56-1068 others(6): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961332 | |||||||
| chr1:9961600 | T | A | 1 | a0001c0001t0004g0150 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-56-10418T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961600 | |||||||
| chr1:9961823 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-56-10195G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961823 | |||||||
| chr1:9961828 | A | C | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-10190A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9961828 | |||||||
| chr1:9962020 | G | C | 1 | a0001c0001t0003g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-9998G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962020 | |||||||
| chr1:9962042 | A | G | 27 | a0001c0001t0002g0009 a0001c0001t0002g0095 a0001c0001t0002g0096 others(24): Show |
30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-56-9976A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962042 | |||||||
| chr1:9962064 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-9954G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962064 | |||||||
| chr1:9962225 | A | G | 1 | a0001c0001t0006g0283 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-56-9793A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962225 | |||||||
| chr1:9962238 | T | C | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-9780T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962238 | |||||||
| chr1:9962481 | GA | G | 34 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0091 others(31): Show |
39 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-9522delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962481 | ||||||
| chr1:9962497 | T | A | 1 | a0001c0001t0003g0058 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-56-9521T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962497 | |||||||
| chr1:9962552 | A | G | 1 | a0001c0001t0027g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-56-9466A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962552 | |||||||
| chr1:9962677 | G | GT | 79 | a0001c0001t0001g0014 a0001c0001t0001g0175 a0001c0001t0001g0176 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-56-9319dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | ||||||
| chr1:9962677 | G | GTT | 49 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 others(46): Show |
49 | HG00597.hp1 HG00597.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-56-9320_-56-9319d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | ||||||
| chr1:9962677 | GT | G | 81 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(78): Show |
96 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(93): Show |
intron_variant | MODIFIER | c.-56-9319delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9962677 | ||||||
| chr1:9962976 | T | C | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-9042T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9962976 | |||||||
| chr1:9963137 | G | C | 55 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(52): Show |
63 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.-56-8881G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963137 | |||||||
| chr1:9963235 | T | C | 122 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(119): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-56-8783T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963235 | |||||||
| chr1:9963333 | C | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-8685C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963333 | |||||||
| chr1:9963643 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0033 others(13): Show |
21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-8375G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963643 | |||||||
| chr1:9963694 | A | C | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-8324A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963694 | |||||||
| chr1:9963696 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | NA18943.hp1 NA18950.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-56-8322C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963696 | |||||||
| chr1:9963792 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-8226C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963792 | |||||||
| chr1:9963830 | T | C | 1 | a0001c0001t0006g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-56-8188T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9963830 | |||||||
| chr1:9964107 | G | T | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-7911G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964107 | |||||||
| chr1:9964144 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-7874G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964144 | |||||||
| chr1:9964196 | G | A | 1 | a0001c0001t0005g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-56-7822G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964196 | |||||||
| chr1:9964206 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-7812A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964206 | |||||||
| chr1:9964219 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0003g0038 |
2 | NA18988.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.-56-7799G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964219 | |||||||
| chr1:9964230 | C | G | 16 | a0001c0001t0004g0006 a0001c0001t0004g0080 a0001c0001t0004g0081 others(13): Show |
17 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-56-7788C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964230 | |||||||
| chr1:9964444 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-56-7574C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964444 | |||||||
| chr1:9964495 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-7523G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964495 | |||||||
| chr1:9964724 | G | A | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-7294G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964724 | |||||||
| chr1:9964821 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-7197A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9964821 | |||||||
| chr1:9964929 | C | CA | 57 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0185 others(54): Show |
61 | HG00099.hp1 HG00438.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.-56-7069dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9964929 | ||||||
| chr1:9964929 | CA | C | 9 | a0001c0001t0001g0176 a0001c0001t0003g0048 a0001c0001t0004g0090 others(6): Show |
9 | HG01070.hp2 HG02559.hp2 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-7069delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9964929 | ||||||
| chr1:9965024 | T | C | 87 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-6994T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965024 | |||||||
| chr1:9965185 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-56-6833C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965185 | |||||||
| chr1:9965189 | G | C | 186 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(183): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-56-6829G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965189 | |||||||
| chr1:9965189 | G | T | 1 | a0001c0001t0005g0258 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-56-6829G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965189 | |||||||
| chr1:9965190 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-56-6828G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965190 | |||||||
| chr1:9965206 | G | A | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-6812G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965206 | |||||||
| chr1:9965315 | C | CA | 21 | a0001c0001t0001g0238 a0001c0001t0001g0263 a0001c0001t0002g0106 others(18): Show |
21 | HG01175.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-6684dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9965315 | ||||||
| chr1:9965369 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-56-6649G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965369 | |||||||
| chr1:9965375 | T | A | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-56-6643T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965375 | |||||||
| chr1:9965517 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0235 |
2 | HG01081.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-56-6501C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965517 | |||||||
| chr1:9965553 | G | A | 3 | a0001c0001t0002g0099 a0001c0001t0002g0103 a0001c0001t0002g0140 |
3 | HG00438.hp2 HG00544.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-56-6465G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965553 | |||||||
| chr1:9965730 | C | T | 27 | a0001c0001t0002g0009 a0001c0001t0002g0095 a0001c0001t0002g0096 others(24): Show |
30 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.-56-6288C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965730 | |||||||
| chr1:9965816 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-56-6202G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965816 | |||||||
| chr1:9965926 | T | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0075 a0001c0001t0002g0091 others(31): Show |
39 | HG00423.hp2 HG00741.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-6092T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965926 | |||||||
| chr1:9965987 | CA | C | 6 | a0001c0001t0002g0095 a0001c0001t0002g0162 a0001c0001t0006g0273 others(3): Show |
6 | HG01884.hp1 HG02615.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-6020delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9965987 | ||||||
| chr1:9965998 | A | T | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-6020A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965998 | |||||||
| chr1:9965999 | T | A | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-6019T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9965999 | |||||||
| chr1:9966248 | G | A | 1 | a0001c0001t0022g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-56-5770G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966248 | |||||||
| chr1:9966339 | G | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0204 a0001c0001t0001g0226 others(5): Show |
8 | HG00280.hp2 HG02293.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-5679G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966339 | |||||||
| chr1:9966365 | C | T | 2 | a0001c0001t0015g0083 a0001c0001t0015g0084 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-56-5653C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9966365 | |||||||
| chr1:9966612 | CA | C | 268 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(265): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-56-5396delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9966612 | ||||||
| chr1:9966612 | CAA | C | 7 | a0001c0001t0003g0039 a0001c0001t0003g0044 a0001c0001t0003g0050 others(4): Show |
7 | HG00408.hp2 HG00544.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-5397_-56-5396d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9966612 | ||||||
| chr1:9967006 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-56-5012C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967006 | |||||||
| chr1:9967130 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-56-4888A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967130 | |||||||
| chr1:9967226 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-56-4792C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967226 | |||||||
| chr1:9967230 | T | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG03704.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-56-4788T>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967230 | |||||||
| chr1:9967231 | C | A | 3 | a0001c0001t0002g0096 a0001c0001t0002g0161 a0001c0001t0002g0162 |
3 | HG03704.hp1 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-56-4787C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967231 | |||||||
| chr1:9967236 | C | CA | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-4772dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9967236 | ||||||
| chr1:9967244 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-56-4774A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967244 | |||||||
| chr1:9967281 | C | G | 1 | a0001c0001t0006g0284 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-56-4737C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967281 | |||||||
| chr1:9967482 | G | A | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(112): Show |
117 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-56-4536G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967482 | |||||||
| chr1:9967556 | T | C | 2 | a0001c0001t0004g0006 a0001c0001t0004g0082 |
3 | HG02559.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-56-4462T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967556 | |||||||
| chr1:9967588 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-4430A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967588 | |||||||
| chr1:9967959 | G | C | 1 | a0001c0001t0004g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-56-4059G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9967959 | |||||||
| chr1:9968021 | A | G | 2 | a0001c0001t0003g0025 a0001c0001t0003g0031 |
2 | HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-3997A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968021 | |||||||
| chr1:9968067 | A | AGTTTTTT others(6): Show |
51 | a0001c0001t0001g0030 a0001c0001t0003g0002 a0001c0001t0003g0003 others(48): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-56-3939_-56-3938i others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968067 | ||||||
| chr1:9968070 | T | TTTTTTTT others(4): Show |
6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3939_-56-3938i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968070 | ||||||
| chr1:9968080 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0005g0205 a0001c0001t0006g0273 a0001c0001t0010g0168 |
3 | HG01256.hp1 NA18983.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(12): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | ||||||
| chr1:9968080 | G | GTTTTTTT others(4): Show |
96 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(93): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | ||||||
| chr1:9968080 | G | GTTTTTTT others(5): Show |
21 | a0001c0001t0001g0197 a0001c0001t0001g0210 a0001c0001t0001g0216 others(18): Show |
21 | HG00438.hp1 HG01123.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(14): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | ||||||
| chr1:9968080 | G | GTTTTTTT others(6): Show |
4 | a0001c0001t0006g0280 a0001c0001t0012g0019 a0001c0001t0012g0020 others(1): Show |
4 | HG00558.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(15): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968080 | ||||||
| chr1:9968080 | G | T | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3938G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968080 | |||||||
| chr1:9968081 | T | TTTTTTTT others(4): Show |
2 | a0001c0001t0001g0257 a0001c0001t0017g0212 |
2 | HG00741.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-56-3929_-56-3928i others(13): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968081 | ||||||
| chr1:9968134 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-3884C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968134 | |||||||
| chr1:9968176 | G | A | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-3842G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968176 | |||||||
| chr1:9968229 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3789G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968229 | |||||||
| chr1:9968293 | C | T | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-3725C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968293 | |||||||
| chr1:9968361 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-56-3657C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968361 | |||||||
| chr1:9968362 | G | A | 7 | a0001c0001t0006g0274 a0001c0001t0006g0275 a0001c0001t0006g0276 others(4): Show |
7 | HG01433.hp1 HG01934.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-3656G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968362 | |||||||
| chr1:9968364 | G | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0093 others(6): Show |
10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-3654G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968364 | |||||||
| chr1:9968431 | A | G | 87 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(84): Show |
97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-56-3587A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968431 | |||||||
| chr1:9968465 | AT | A | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 |
3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-3551delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968465 | ||||||
| chr1:9968512 | A | G | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3506A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968512 | |||||||
| chr1:9968514 | G | C | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-3504G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968514 | |||||||
| chr1:9968518 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-56-3500A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968518 | |||||||
| chr1:9968533 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-3485G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968533 | |||||||
| chr1:9968551 | A | AAGGTCAG others(134): Show |
5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3457_-56-3456i others(143): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | ||||||
| chr1:9968551 | A | AAGGTCAG others(134): Show |
1 | a0001c0001t0013g0046 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-56-3457_-56-3456i others(143): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | ||||||
| chr1:9968551 | A | AAGGTCAG others(133): Show |
181 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(178): Show |
191 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.-56-3457_-56-3456i others(142): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968551 | ||||||
| chr1:9968596 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3422G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968596 | |||||||
| chr1:9968632 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3386G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968632 | |||||||
| chr1:9968770 | C | CA | 136 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(133): Show |
139 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-56-3229dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968770 | ||||||
| chr1:9968939 | C | CA | 39 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0001g0202 others(36): Show |
42 | HG00438.hp2 HG00544.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-56-3062dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968939 | ||||||
| chr1:9968939 | C | CAA | 6 | a0001c0001t0003g0066 a0001c0001t0012g0018 a0001c0001t0012g0019 others(3): Show |
6 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-3063_-56-3062d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9968939 | ||||||
| chr1:9968973 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-3045G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9968973 | |||||||
| chr1:9969336 | G | T | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-2682G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969336 | |||||||
| chr1:9969417 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-56-2601A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969417 | |||||||
| chr1:9969423 | A | G | 5 | a0001c0001t0004g0146 a0001c0001t0004g0147 a0001c0001t0004g0148 others(2): Show |
5 | HG01109.hp1 HG01257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-2595A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969423 | |||||||
| chr1:9969496 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-2522G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969496 | |||||||
| chr1:9969550 | G | A | 1 | a0001c0001t0018g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-56-2468G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969550 | |||||||
| chr1:9969705 | C | G | 1 | a0001c0001t0027g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-56-2313C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969705 | |||||||
| chr1:9969752 | A | G | 1 | a0001c0001t0002g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-56-2266A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969752 | |||||||
| chr1:9969855 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-2163A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969855 | |||||||
| chr1:9969955 | G | A | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-56-2063G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969955 | |||||||
| chr1:9969974 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-56-2044C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9969974 | |||||||
| chr1:9970153 | G | T | 2 | a0001c0001t0002g0109 a0001c0001t0002g0138 |
2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-56-1865G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970153 | |||||||
| chr1:9970249 | A | G | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-56-1769A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970249 | |||||||
| chr1:9970379 | C | CTA | 9 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0093 others(6): Show |
10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-1631_-56-1630d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9970379 | ||||||
| chr1:9970546 | A | C | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-1472A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970546 | |||||||
| chr1:9970572 | C | G | 1 | a0001c0001t0002g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-56-1446C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970572 | |||||||
| chr1:9970685 | G | A | 3 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 |
3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-56-1333G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970685 | |||||||
| chr1:9970712 | A | C | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-56-1306A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970712 | |||||||
| chr1:9970899 | A | T | 2 | a0001c0001t0015g0083 a0001c0001t0015g0084 |
2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-56-1119A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9970899 | |||||||
| chr1:9971030 | TTGGGTTT others(16): Show |
T | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-987_-56-965del others(23): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971030 | |||||||
| chr1:9971248 | G | A | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-56-770G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971248 | |||||||
| chr1:9971354 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-56-664G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971354 | |||||||
| chr1:9971378 | G | A | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-56-640G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971378 | |||||||
| chr1:9971482 | T | C | 2 | a0001c0001t0006g0272 a0001c0001t0006g0282 |
2 | HG02074.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-56-536T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971482 | |||||||
| chr1:9971572 | A | G | 1 | a0001c0001t0004g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-56-446A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | chr1 | 9971572 | |||||||
| chr1:9971973 | G | GA | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-36dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 9971973 | ||||||
| chr1:9972233 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+45G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972233 | |||||||
| chr1:9972410 | C | T | 1 | a0001c0001t0004g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115+222C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972410 | |||||||
| chr1:9972420 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+232C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972420 | |||||||
| chr1:9972486 | C | T | 1 | a0001c0001t0008g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115+298C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972486 | |||||||
| chr1:9972494 | C | CA | 79 | a0001c0001t0001g0030 a0001c0001t0001g0191 a0001c0001t0001g0222 others(76): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.115+321dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | ||||||
| chr1:9972494 | C | CAA | 193 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0175 others(190): Show |
205 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.115+320_115+321dup others(2): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | ||||||
| chr1:9972494 | C | CAAA | 8 | a0001c0001t0002g0098 a0001c0001t0002g0106 a0001c0001t0002g0167 others(5): Show |
8 | HG02083.hp2 HG02132.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+319_115+321dup others(3): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9972494 | ||||||
| chr1:9972571 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.115+383A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972571 | |||||||
| chr1:9972756 | G | A | 3 | a0001c0001t0011g0223 a0001c0001t0011g0224 a0001c0001t0011g0225 |
3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.115+568G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972756 | |||||||
| chr1:9972947 | C | A | 1 | a0001c0001t0001g0220 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.115+759C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9972947 | |||||||
| chr1:9973175 | G | C | 1 | a0001c0001t0003g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+987G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973175 | |||||||
| chr1:9973307 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.115+1119G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973307 | |||||||
| chr1:9973416 | C | T | 9 | a0001c0001t0002g0010 a0001c0001t0002g0092 a0001c0001t0002g0093 others(6): Show |
10 | HG01167.hp2 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+1228C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973416 | |||||||
| chr1:9973434 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115+1246G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973434 | |||||||
| chr1:9973707 | C | CA | 53 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0001g0216 others(50): Show |
55 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.115+1544dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | ||||||
| chr1:9973707 | C | CAA | 11 | a0001c0001t0002g0135 a0001c0001t0004g0082 a0001c0001t0004g0085 others(8): Show |
11 | HG00597.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.115+1543_115+1544d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | ||||||
| chr1:9973707 | CA | C | 59 | a0001c0001t0001g0195 a0001c0001t0001g0222 a0001c0001t0002g0009 others(56): Show |
69 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.115+1544delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | ||||||
| chr1:9973707 | CAAA | C | 6 | a0001c0001t0004g0080 a0001c0001t0004g0081 a0001c0001t0008g0170 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.115+1542_115+1544d others(5): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9973707 | ||||||
| chr1:9973777 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+1589C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973777 | |||||||
| chr1:9973868 | C | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.115+1680C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973868 | |||||||
| chr1:9973884 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115+1696C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973884 | |||||||
| chr1:9973961 | C | G | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-1631C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973961 | |||||||
| chr1:9973998 | C | T | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.116-1594C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9973998 | |||||||
| chr1:9974217 | A | AT | 13 | a0001c0001t0001g0263 a0001c0001t0002g0131 a0001c0001t0002g0160 others(10): Show |
13 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.116-1360dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974217 | ||||||
| chr1:9974327 | G | A | 1 | a0001c0001t0004g0289 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.116-1265G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974327 | |||||||
| chr1:9974371 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.116-1221A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974371 | |||||||
| chr1:9974390 | A | AT | 266 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(263): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.116-1187dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974390 | ||||||
| chr1:9974390 | A | ATT | 9 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0231 others(6): Show |
9 | HG00408.hp1 HG01255.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-1188_116-1187d others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 9974390 | ||||||
| chr1:9974538 | G | A | 1 | a0001c0001t0006g0280 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.116-1054G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974538 | |||||||
| chr1:9974797 | A | T | 289 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(286): Show |
310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.116-795A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974797 | |||||||
| chr1:9974825 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.116-767C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974825 | |||||||
| chr1:9974931 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116-661A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974931 | |||||||
| chr1:9974992 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.116-600G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9974992 | |||||||
| chr1:9975023 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0221 |
2 | HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.116-569G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975023 | |||||||
| chr1:9975374 | G | T | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.116-218G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975374 | |||||||
| chr1:9975380 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.116-212A>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975380 | |||||||
| chr1:9975415 | T | C | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.116-177T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975415 | |||||||
| chr1:9975450 | G | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0050 |
2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.116-142G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 2/4 | chr1 | 9975450 | |||||||
| chr1:9975859 | A | G | 3 | a0001c0001t0004g0144 a0001c0001t0004g0152 a0001c0001t0004g0153 |
3 | HG03139.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.299+84A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9975859 | |||||||
| chr1:9975951 | G | A | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(53): Show |
64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.299+176G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9975951 | |||||||
| chr1:9976156 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+381G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976156 | |||||||
| chr1:9976274 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+499G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976274 | |||||||
| chr1:9976286 | C | CA | 8 | a0001c0001t0001g0175 a0001c0001t0001g0226 a0001c0001t0001g0264 others(5): Show |
8 | HG00280.hp2 HG01433.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.299+530dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976286 | ||||||
| chr1:9976286 | CA | C | 13 | a0001c0001t0001g0190 a0001c0001t0002g0075 a0001c0001t0002g0113 others(10): Show |
13 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.299+530delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976286 | ||||||
| chr1:9976307 | A | T | 1 | a0001c0001t0004g0090 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.299+532A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976307 | |||||||
| chr1:9976469 | A | T | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+694A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976469 | |||||||
| chr1:9976470 | G | A | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+695G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976470 | |||||||
| chr1:9976471 | C | A | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+696C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976471 | |||||||
| chr1:9976472 | A | T | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+697A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976472 | |||||||
| chr1:9976474 | C | T | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+699C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976474 | |||||||
| chr1:9976475 | C | A | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+700C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976475 | |||||||
| chr1:9976477 | GTGCT | G | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+703_299+706del others(4): Show |
NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976477 | |||||||
| chr1:9976484 | T | C | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+709T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976484 | |||||||
| chr1:9976487 | A | T | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+712A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976487 | |||||||
| chr1:9976488 | T | C | 13 | a0001c0001t0002g0125 a0001c0001t0005g0243 a0001c0001t0005g0244 others(10): Show |
13 | HG00597.hp2 HG01943.hp1 NA18951.hp2 others(10): Show |
intron_variant | MODIFIER | c.299+713T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976488 | |||||||
| chr1:9976681 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299+906G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976681 | |||||||
| chr1:9976889 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299+1114C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976889 | |||||||
| chr1:9976912 | C | CT | 64 | a0001c0001t0001g0199 a0001c0001t0001g0263 a0001c0001t0003g0002 others(61): Show |
72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.299+1148dupT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9976912 | ||||||
| chr1:9976929 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.299+1154A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9976929 | |||||||
| chr1:9977033 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.299+1258A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977033 | |||||||
| chr1:9977068 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+1293G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977068 | |||||||
| chr1:9977148 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.299+1373C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977148 | |||||||
| chr1:9977161 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.299+1386G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977161 | |||||||
| chr1:9977178 | G | C | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+1403G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977178 | |||||||
| chr1:9977399 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0107 a0001c0001t0002g0126 |
3 | NA18990.hp2 NA19001.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.299+1624T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977399 | |||||||
| chr1:9977410 | A | T | 115 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(112): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.299+1635A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977410 | |||||||
| chr1:9977588 | C | G | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.299+1813C>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977588 | |||||||
| chr1:9977589 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.299+1814G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977589 | |||||||
| chr1:9977621 | C | T | 1 | a0001c0001t0019g0290 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.299+1846C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977621 | |||||||
| chr1:9977640 | G | A | 2 | a0001c0001t0007g0076 a0001c0001t0007g0078 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.299+1865G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977640 | |||||||
| chr1:9977868 | C | A | 1 | a0001c0001t0002g0140 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.299+2093C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9977868 | |||||||
| chr1:9978081 | G | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+2306G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978081 | |||||||
| chr1:9978312 | C | T | 1 | a0001c0001t0027g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.299+2537C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978312 | |||||||
| chr1:9978341 | G | A | 1 | a0001c0001t0018g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.299+2566G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978341 | |||||||
| chr1:9978351 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.299+2576G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978351 | |||||||
| chr1:9978360 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0033 others(13): Show |
21 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.299+2585A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978360 | |||||||
| chr1:9978379 | C | T | 2 | a0001c0001t0014g0017 a0001c0001t0014g0021 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299+2604C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978379 | |||||||
| chr1:9978427 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300-2604T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978427 | |||||||
| chr1:9978459 | G | A | 1 | a0004c0003t0021g0015 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.300-2572G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978459 | |||||||
| chr1:9978597 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.300-2434C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978597 | |||||||
| chr1:9978629 | G | A | 1 | a0001c0001t0005g0255 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.300-2402G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978629 | |||||||
| chr1:9978659 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.300-2372C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978659 | |||||||
| chr1:9978870 | C | T | 2 | a0001c0001t0004g0085 a0001c0001t0004g0090 |
2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.300-2161C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978870 | |||||||
| chr1:9978947 | C | T | 1 | a0001c0001t0016g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.300-2084C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9978947 | |||||||
| chr1:9979061 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.300-1970G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979061 | |||||||
| chr1:9979089 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.300-1942T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979089 | |||||||
| chr1:9979161 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.300-1870C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979161 | |||||||
| chr1:9979304 | C | A | 279 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.300-1727C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979304 | |||||||
| chr1:9979533 | G | T | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.300-1498G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979533 | |||||||
| chr1:9979627 | T | C | 2 | a0001c0001t0004g0145 a0001c0001t0004g0151 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.300-1404T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979627 | |||||||
| chr1:9979760 | C | T | 1 | a0001c0001t0003g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.300-1271C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9979760 | |||||||
| chr1:9979801 | C | CA | 15 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0209 others(12): Show |
15 | HG00639.hp2 HG01255.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.300-1213dupA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979801 | ||||||
| chr1:9979801 | CA | C | 7 | a0001c0001t0002g0098 a0001c0001t0008g0032 a0001c0001t0008g0170 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.300-1213delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979801 | ||||||
| chr1:9979933 | AT | A | 31 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0176 others(28): Show |
32 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.300-1088delT | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9979933 | ||||||
| chr1:9980152 | G | A | 5 | a0001c0001t0010g0022 a0001c0001t0010g0168 a0001c0001t0010g0169 others(2): Show |
5 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.300-879G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980152 | |||||||
| chr1:9980191 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.300-840C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980191 | |||||||
| chr1:9980372 | A | T | 1 | a0001c0001t0003g0024 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.300-659A>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980372 | |||||||
| chr1:9980451 | A | G | 187 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(184): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.300-580A>G | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980451 | |||||||
| chr1:9980464 | CA | C | 276 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(273): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.300-558delA | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 9980464 | ||||||
| chr1:9980494 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.300-537G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980494 | |||||||
| chr1:9980683 | G | C | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-348G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980683 | |||||||
| chr1:9980710 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.300-321G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980710 | |||||||
| chr1:9980728 | C | T | 1 | a0001c0001t0018g0070 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.300-303C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 3/4 | chr1 | 9980728 | |||||||
| chr1:9981195 | C | T | 2 | a0001c0001t0004g0085 a0001c0001t0004g0090 |
2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.439+25C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981195 | |||||||
| chr1:9981238 | G | C | 1 | a0001c0001t0004g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.439+68G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981238 | |||||||
| chr1:9981393 | C | A | 5 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(2): Show |
5 | HG02922.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+223C>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981393 | |||||||
| chr1:9981527 | G | A | 7 | a0001c0001t0012g0018 a0001c0001t0012g0019 a0001c0001t0012g0020 others(4): Show |
7 | HG01884.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+357G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981527 | |||||||
| chr1:9981598 | T | C | 1 | a0001c0001t0005g0205 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.439+428T>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981598 | |||||||
| chr1:9981695 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.439+525C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981695 | |||||||
| chr1:9981762 | G | A | 1 | a0001c0001t0006g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.440-539G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981762 | |||||||
| chr1:9981908 | G | T | 6 | a0001c0001t0008g0032 a0001c0001t0008g0170 a0001c0001t0008g0171 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-393G>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981908 | |||||||
| chr1:9981919 | G | A | 119 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(116): Show |
121 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.440-382G>A | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981919 | |||||||
| chr1:9981956 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.440-345C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9981956 | |||||||
| chr1:9982006 | G | C | 1 | a0001c0001t0020g0027 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.440-295G>C | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9982006 | |||||||
| chr1:9982075 | C | T | 56 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0004 others(53): Show |
64 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.440-226C>T | NMNAT1 | ENSG00000173614.14 | transcript | ENST00000377205.6 | protein_coding | 4/4 | chr1 | 9982075 |