Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 349565 |
| ensemblid | ENSG00000163864.18 |
| hgncid | 20989 |
| symbol | NMNAT3 |
| name | nicotinamide nucleotide adenylyltransferase 3 |
| refseq_nuc | NM_001401600.1 |
| refseq_prot | NP_001388529.1 |
| ensembl_nuc | ENST00000704800.1 |
| ensembl_prot | ENSP00000516041.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 139560191 |
| end | 139677972 |
| strand | - |
| ver | v1.2 |
| region | chr3:139560191-139677972 |
| region5000 | chr3:139555191-139682972 |
| regionname0 | NMNAT3_chr3_139560191_139677972 |
| regionname5000 | NMNAT3_chr3_139555191_139682972 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 252 | 319 | 84 | 64 | 120 | 16 | 33 | 90 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | MKSRI others(247): Show |
chr3 | 139555191 | 139682972 |
| a0002 | 0/0 | 252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | MKSRI others(247): Show |
chr3 | 139555191 | 139682972 |
| a0003 | 0/0 | 252 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | MKSRI others(247): Show |
chr3 | 139555191 | 139682972 |
| a0004 | 0/0 | 252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | MKSRI others(247): Show |
chr3 | 139555191 | 139682972 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 756 | 301 | 71 | 60 | 120 | 16 | 32 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0001c0002 | 0/0 | 756 | 9 | 7 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0001c0003 | 0/0 | 756 | 6 | 4 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0001c0004 | 0/0 | 756 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0001c0007 | 0/0 | 756 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0002c0005 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0003c0006 | 0/0 | 756 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 | ||
| a0004c0008 | 0/0 | 756 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | ATGAA others(751): Show |
chr3 | 139555191 | 139682972 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2023 | 204 | 41 | 36 | 94 | 11 | 22 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0002 | 0/1 | 2023 | 80 | 25 | 18 | 21 | 5 | 10 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0003 | 0/0 | 2023 | 5 | 2 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0004 | 0/0 | 2023 | 3 | 0 | 3 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0005 | 0/0 | 2023 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0006 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0007 | 1/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0008 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0009 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0010 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0011 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0001t0012 | 0/0 | 2023 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0002t0001 | 0/0 | 2023 | 5 | 4 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0002t0002 | 0/0 | 2023 | 4 | 3 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0003t0001 | 0/0 | 2023 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0003t0002 | 0/0 | 2023 | 4 | 3 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0004t0001 | 0/0 | 2023 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0001c0007t0001 | 0/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0002c0005t0002 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0003c0006t0001 | 0/0 | 2023 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| a0004c0008t0001 | 0/0 | 2023 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | AGACT others(2018): Show |
chr3 | 139555191 | 139682972 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0007g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0001t0012g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0004t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0001c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0002c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0003c0006t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| a0004c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | GBR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | FIN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0192 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0035 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0094 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0089 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0103 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0119 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02965 | hp1 | a0002 | c0005 | t0002 | g0033 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0122 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03492 | hp2 | a0001 | c0007 | t0001 | g0262 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03942 | hp2 | a0003 | c0006 | t0001 | g0261 | SAS | BEB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18953 | hp1 | a0001 | c0001 | t0010 | g0227 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0268 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18980 | hp2 | a0001 | c0001 | t0012 | g0238 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0299 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19030 | hp2 | a0004 | c0008 | t0001 | g0159 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19062 | hp1 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | GIH | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0090 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0019 | AFR | ACB | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0177 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0147 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0037 | REF | REF | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0020 | REF | REF | NMNAT3_chr3_139555191_139682972 | NMNAT3 | chr3 | 139555191 | 139682972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139573651 | G | A | 1 | a0002 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.323C>T | p.Pro108Leu | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 768/2023 | 323/759 | 108/252 | chr3 | 139573651 | |||
| chr3:139573652 | G | A | 1 | a0002 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.322C>T | p.Pro108Ser | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 767/2023 | 322/759 | 108/252 | chr3 | 139573652 | |||
| chr3:139573668 | G | C | 1 | a0003 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.306C>G | p.Ser102Arg | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/7 | 751/2023 | 306/759 | 102/252 | chr3 | 139573668 | |||
| chr3:139627708 | G | C | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.17C>G | p.Pro6Arg | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/7 | 462/2023 | 17/759 | 6/252 | chr3 | 139627708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139561094 | C | T | 1 | a0001c0003 | 6 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(3): Show |
synonymous_variant | LOW | c.675G>A | p.Thr225Thr | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 1120/2023 | 675/759 | 225/252 | chr3 | 139561094 | |||
| chr3:139561109 | G | A | 1 | a0001c0004 | 2 | HG02896.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.660C>T | p.Pro220Pro | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 1105/2023 | 660/759 | 220/252 | chr3 | 139561109 | |||
| chr3:139578991 | G | A | 1 | a0001c0002 | 9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
synonymous_variant | LOW | c.174C>T | p.Leu58Leu | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/7 | 619/2023 | 174/759 | 58/252 | chr3 | 139578991 | |||
| chr3:139579015 | G | A | 1 | a0001c0007 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.150C>T | p.Asn50Asn | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/7 | 595/2023 | 150/759 | 50/252 | chr3 | 139579015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139560279 | C | T | 1 | a0001c0001t0009 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 731 | chr3 | 139560279 | ||||||
| chr3:139560350 | T | C | 1 | a0001c0001t0010 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 660 | chr3 | 139560350 | ||||||
| chr3:139560431 | A | G | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(16): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*579T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 579 | chr3 | 139560431 | ||||||
| chr3:139560690 | C | T | 1 | a0001c0001t0008 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 320 | chr3 | 139560690 | ||||||
| chr3:139560847 | G | A | 1 | a0001c0001t0011 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 163 | chr3 | 139560847 | ||||||
| chr3:139560860 | G | A | 1 | a0001c0001t0012 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 150 | chr3 | 139560860 | ||||||
| chr3:139560874 | C | T | 1 | a0001c0001t0006 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*136G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 7/7 | 136 | chr3 | 139560874 | ||||||
| chr3:139677892 | T | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
231 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
5_prime_UTR_variant | MODIFIER | c.-365A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | 50168 | chr3 | 139677892 | ||||||
| chr3:139677916 | G | A | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(11): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-389C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | chr3 | 139677916 | |||||||
| chr3:139677958 | G | T | 1 | a0001c0001t0005 | 2 | HG03453.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-431C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/7 | 50234 | chr3 | 139677958 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:139561486 | G | GA | 269 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(266): Show |
276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.377-95dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561486 | |||||||
| chr3:139561580 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.377-188A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561580 | |||||||
| chr3:139561617 | A | G | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-225T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561617 | |||||||
| chr3:139561634 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.377-242G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561634 | |||||||
| chr3:139561794 | C | A | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.377-402G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561794 | |||||||
| chr3:139561843 | A | G | 85 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0132 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-451T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561843 | |||||||
| chr3:139561990 | GT | G | 30 | a0001c0001t0001g0008 a0001c0001t0001g0131 a0001c0001t0001g0141 others(27): Show |
31 | HG01192.hp1 HG02027.hp2 HG02165.hp2 others(28): Show |
intron_variant | MODIFIER | c.377-599delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139561990 | |||||||
| chr3:139562090 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-698G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562090 | |||||||
| chr3:139562127 | A | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0276 |
2 | NA18978.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.377-735T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562127 | |||||||
| chr3:139562142 | A | ATTG | 85 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0132 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-753_377-751dup others(3): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562142 | |||||||
| chr3:139562311 | C | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.377-919G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562311 | |||||||
| chr3:139562349 | C | G | 85 | a0001c0001t0001g0115 a0001c0001t0001g0127 a0001c0001t0001g0132 others(82): Show |
85 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.377-957G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562349 | |||||||
| chr3:139562370 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-978C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562370 | |||||||
| chr3:139562750 | A | G | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.377-1358T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562750 | |||||||
| chr3:139562994 | C | T | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0167 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.377-1602G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139562994 | |||||||
| chr3:139563026 | T | C | 4 | a0001c0001t0001g0293 a0001c0001t0002g0022 a0001c0001t0002g0075 others(1): Show |
4 | HG02027.hp2 NA18953.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-1634A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563026 | |||||||
| chr3:139563060 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.377-1668A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563060 | |||||||
| chr3:139563074 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.377-1682A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563074 | |||||||
| chr3:139563344 | C | A | 79 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-1952G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563344 | |||||||
| chr3:139563538 | C | T | 263 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(260): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.377-2146G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563538 | |||||||
| chr3:139563544 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.377-2152T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563544 | |||||||
| chr3:139563618 | T | C | 4 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(1): Show |
4 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-2226A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563618 | |||||||
| chr3:139563709 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.377-2317G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563709 | |||||||
| chr3:139563728 | G | C | 81 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.377-2336C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563728 | |||||||
| chr3:139563733 | A | G | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0167 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.377-2341T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563733 | |||||||
| chr3:139563739 | G | A | 79 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-2347C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563739 | |||||||
| chr3:139563856 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0223 a0001c0001t0012g0238 |
3 | NA18962.hp2 NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.377-2464C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563856 | |||||||
| chr3:139563861 | C | A | 80 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.377-2469G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563861 | |||||||
| chr3:139563865 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-2473A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563865 | |||||||
| chr3:139563966 | A | G | 267 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.377-2574T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139563966 | |||||||
| chr3:139564147 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.377-2755T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564147 | |||||||
| chr3:139564224 | C | A | 2 | a0001c0001t0002g0092 a0001c0001t0006g0044 |
2 | HG01169.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.377-2832G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564224 | |||||||
| chr3:139564245 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.377-2853G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564245 | |||||||
| chr3:139564266 | G | GT | 14 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.377-2875dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564266 | |||||||
| chr3:139564372 | T | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-2980A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564372 | |||||||
| chr3:139564391 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | NA18993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.377-2999G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564391 | |||||||
| chr3:139564552 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-3160G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564552 | |||||||
| chr3:139564558 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.377-3166G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564558 | |||||||
| chr3:139564562 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-3170G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564562 | |||||||
| chr3:139564620 | A | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
184 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.377-3228T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564620 | |||||||
| chr3:139564915 | CAAT | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0223 a0001c0001t0001g0249 others(3): Show |
6 | NA18962.hp2 NA18972.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.377-3526_377-3524d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139564915 | |||||||
| chr3:139565005 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-3613T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565005 | |||||||
| chr3:139565131 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.377-3739C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565131 | |||||||
| chr3:139565162 | A | G | 14 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.377-3770T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565162 | |||||||
| chr3:139565192 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-3800A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565192 | |||||||
| chr3:139565428 | C | T | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
176 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.377-4036G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565428 | |||||||
| chr3:139565489 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.377-4097A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565489 | |||||||
| chr3:139565514 | T | G | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-4122A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565514 | |||||||
| chr3:139565515 | C | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.377-4123G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565515 | |||||||
| chr3:139565547 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.377-4155C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565547 | |||||||
| chr3:139565574 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.377-4182G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565574 | |||||||
| chr3:139565608 | C | T | 2 | a0001c0001t0001g0313 a0001c0001t0002g0028 |
2 | HG03516.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.377-4216G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565608 | |||||||
| chr3:139565654 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
80 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-4262A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565654 | |||||||
| chr3:139565716 | A | T | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.377-4324T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565716 | |||||||
| chr3:139565894 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.377-4502C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139565894 | |||||||
| chr3:139566046 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.377-4654A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566046 | |||||||
| chr3:139566047 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.377-4655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566047 | |||||||
| chr3:139566048 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.377-4656C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566048 | |||||||
| chr3:139566170 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.377-4778C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566170 | |||||||
| chr3:139566180 | A | C | 74 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(71): Show |
75 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.377-4788T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566180 | |||||||
| chr3:139566182 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-4790T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566182 | |||||||
| chr3:139566309 | A | G | 268 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(265): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.377-4917T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566309 | |||||||
| chr3:139566339 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0312 |
2 | HG00423.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.377-4947A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566339 | |||||||
| chr3:139566344 | T | A | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
160 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.377-4952A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566344 | |||||||
| chr3:139566557 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5165T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566557 | |||||||
| chr3:139566644 | C | G | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
179 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.377-5252G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566644 | |||||||
| chr3:139566718 | C | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
80 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.377-5326G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566718 | |||||||
| chr3:139566734 | G | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
179 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.377-5342C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566734 | |||||||
| chr3:139566844 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.377-5452C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566844 | |||||||
| chr3:139566889 | A | G | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.377-5497T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566889 | |||||||
| chr3:139566922 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.377-5530T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566922 | |||||||
| chr3:139566928 | C | T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.377-5536G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139566928 | |||||||
| chr3:139567089 | A | C | 122 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(119): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.377-5697T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567089 | |||||||
| chr3:139567250 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.377-5858T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567250 | |||||||
| chr3:139567267 | G | A | 79 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.377-5875C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567267 | |||||||
| chr3:139567298 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5906A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567298 | |||||||
| chr3:139567336 | C | G | 1 | a0001c0001t0001g0296 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.377-5944G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567336 | |||||||
| chr3:139567368 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377-5976A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567368 | |||||||
| chr3:139567438 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.377-6046G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567438 | |||||||
| chr3:139567468 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.377-6076G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567468 | |||||||
| chr3:139567654 | C | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0230 |
2 | NA18970.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.376+5944G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567654 | |||||||
| chr3:139567655 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.376+5943T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567655 | |||||||
| chr3:139567770 | G | A | 19 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.376+5828C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567770 | |||||||
| chr3:139567851 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.376+5747G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567851 | |||||||
| chr3:139567866 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.376+5732T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139567866 | |||||||
| chr3:139568117 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376+5481C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568117 | |||||||
| chr3:139568334 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+5264G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568334 | |||||||
| chr3:139568338 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.376+5260A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568338 | |||||||
| chr3:139568449 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.376+5149C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568449 | |||||||
| chr3:139568465 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.376+5133C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568465 | |||||||
| chr3:139568530 | T | C | 5 | a0001c0001t0001g0118 a0001c0001t0001g0174 a0001c0001t0001g0180 others(2): Show |
5 | HG02559.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.376+5068A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568530 | |||||||
| chr3:139568552 | C | A | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
180 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.376+5046G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568552 | |||||||
| chr3:139568553 | A | G | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(174): Show |
183 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.376+5045T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568553 | |||||||
| chr3:139568595 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.376+5003T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568595 | |||||||
| chr3:139568630 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0275 |
2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.376+4968C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568630 | |||||||
| chr3:139568642 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.376+4956G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568642 | |||||||
| chr3:139568647 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376+4951G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568647 | |||||||
| chr3:139568766 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.376+4832C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568766 | |||||||
| chr3:139568782 | T | C | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376+4816A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139568782 | |||||||
| chr3:139569011 | T | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(71): Show |
intron_variant | MODIFIER | c.376+4587A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569011 | |||||||
| chr3:139569115 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0264 |
2 | HG00323.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.376+4483A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569115 | |||||||
| chr3:139569179 | GTT | G | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+4417_376+4418d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569179 | |||||||
| chr3:139569201 | C | G | 253 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+4397G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569201 | |||||||
| chr3:139569272 | C | CTGA | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.376+4323_376+4325d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569272 | |||||||
| chr3:139569490 | C | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0285 |
2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.376+4108G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569490 | |||||||
| chr3:139569530 | C | G | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+4068G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569530 | |||||||
| chr3:139569702 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+3896G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569702 | |||||||
| chr3:139569722 | T | A | 1 | a0001c0001t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.376+3876A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569722 | |||||||
| chr3:139569749 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.376+3849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569749 | |||||||
| chr3:139569830 | C | T | 4 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(1): Show |
4 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+3768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569830 | |||||||
| chr3:139569945 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.376+3653C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569945 | |||||||
| chr3:139569962 | C | T | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
177 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.376+3636G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569962 | |||||||
| chr3:139569997 | G | T | 9 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0179 others(6): Show |
9 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+3601C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139569997 | |||||||
| chr3:139570130 | C | T | 5 | a0001c0001t0001g0301 a0001c0002t0001g0120 a0001c0002t0001g0122 others(2): Show |
5 | HG01175.hp1 HG02273.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.376+3468G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570130 | |||||||
| chr3:139570142 | T | C | 10 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0167 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.376+3456A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570142 | |||||||
| chr3:139570145 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376+3453C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570145 | |||||||
| chr3:139570319 | G | T | 94 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.376+3279C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570319 | |||||||
| chr3:139570458 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.376+3140A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570458 | |||||||
| chr3:139570459 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0002g0023 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+3139G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570459 | |||||||
| chr3:139570571 | C | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.376+3027G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570571 | |||||||
| chr3:139570607 | C | A | 93 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.376+2991G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570607 | |||||||
| chr3:139570692 | G | A | 77 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(74): Show |
77 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.376+2906C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570692 | |||||||
| chr3:139570699 | T | C | 9 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0179 others(6): Show |
9 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+2899A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570699 | |||||||
| chr3:139570748 | C | T | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376+2850G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570748 | |||||||
| chr3:139570776 | C | T | 93 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.376+2822G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570776 | |||||||
| chr3:139570956 | G | T | 94 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(91): Show |
95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.376+2642C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139570956 | |||||||
| chr3:139571010 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.376+2588G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571010 | |||||||
| chr3:139571011 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+2587C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571011 | |||||||
| chr3:139571036 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.376+2562T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571036 | |||||||
| chr3:139571040 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.376+2558G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571040 | |||||||
| chr3:139571049 | C | T | 1 | a0001c0003t0002g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.376+2549G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571049 | |||||||
| chr3:139571143 | C | T | 20 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.376+2455G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571143 | |||||||
| chr3:139571178 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2420C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571178 | |||||||
| chr3:139571201 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2397G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571201 | |||||||
| chr3:139571202 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.376+2396C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571202 | |||||||
| chr3:139571240 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2358G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571240 | |||||||
| chr3:139571324 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2274G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571324 | |||||||
| chr3:139571335 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.376+2263G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571335 | |||||||
| chr3:139571336 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376+2262C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571336 | |||||||
| chr3:139571388 | T | C | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376+2210A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571388 | |||||||
| chr3:139571426 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.376+2172C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571426 | |||||||
| chr3:139571476 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.376+2122G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571476 | |||||||
| chr3:139571477 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+2121C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571477 | |||||||
| chr3:139571513 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.376+2085G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571513 | |||||||
| chr3:139571602 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.376+1996T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571602 | |||||||
| chr3:139571627 | C | T | 81 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+1971G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571627 | |||||||
| chr3:139571683 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.376+1915C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571683 | |||||||
| chr3:139571746 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0286 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+1852G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571746 | |||||||
| chr3:139571776 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.376+1822G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571776 | |||||||
| chr3:139571938 | C | A | 1 | a0001c0001t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.376+1660G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571938 | |||||||
| chr3:139571955 | C | T | 14 | a0001c0001t0001g0105 a0001c0001t0001g0115 a0001c0001t0001g0121 others(11): Show |
15 | HG01109.hp1 HG01175.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.376+1643G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571955 | |||||||
| chr3:139571969 | A | G | 81 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+1629T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139571969 | |||||||
| chr3:139572085 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.376+1513G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572085 | |||||||
| chr3:139572102 | C | A | 1 | a0001c0001t0006g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.376+1496G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572102 | |||||||
| chr3:139572129 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.376+1469C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572129 | |||||||
| chr3:139572378 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.376+1220T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572378 | |||||||
| chr3:139572492 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0002g0023 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.376+1106G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572492 | |||||||
| chr3:139572575 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376+1023C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572575 | |||||||
| chr3:139572768 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.376+830G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572768 | |||||||
| chr3:139572831 | A | G | 81 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.376+767T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572831 | |||||||
| chr3:139572907 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.376+691G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572907 | |||||||
| chr3:139572964 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.376+634G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572964 | |||||||
| chr3:139572973 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+625C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139572973 | |||||||
| chr3:139573045 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0002g0023 others(1): Show |
4 | HG02145.hp1 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.376+553G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573045 | |||||||
| chr3:139573180 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0083 |
2 | NA18980.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.376+418G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573180 | |||||||
| chr3:139573238 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.376+360C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573238 | |||||||
| chr3:139573254 | A | G | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.376+344T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573254 | |||||||
| chr3:139573493 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.376+105C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573493 | |||||||
| chr3:139573541 | G | T | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.376+57C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 6/6 | chr3 | 139573541 | |||||||
| chr3:139573953 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.294-273G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139573953 | |||||||
| chr3:139573972 | CA | C | 11 | a0001c0001t0001g0118 a0001c0001t0001g0235 a0001c0002t0001g0120 others(8): Show |
12 | HG01123.hp1 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.294-293delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139573972 | |||||||
| chr3:139574246 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.294-566G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574246 | |||||||
| chr3:139574266 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.294-586G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574266 | |||||||
| chr3:139574311 | C | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
158 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.294-631G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574311 | |||||||
| chr3:139574500 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.294-820A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574500 | |||||||
| chr3:139574892 | A | T | 1 | a0001c0001t0002g0012 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.294-1212T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139574892 | |||||||
| chr3:139575101 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.294-1421A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575101 | |||||||
| chr3:139575268 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.294-1588C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575268 | |||||||
| chr3:139575363 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294-1683G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575363 | |||||||
| chr3:139575430 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.294-1750G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575430 | |||||||
| chr3:139575641 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.294-1961A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575641 | |||||||
| chr3:139575674 | C | T | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.294-1994G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139575674 | |||||||
| chr3:139576137 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.294-2457C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576137 | |||||||
| chr3:139576220 | A | AT | 6 | a0001c0001t0001g0212 a0001c0001t0001g0253 a0001c0001t0001g0304 others(3): Show |
6 | NA18612.hp1 NA18946.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.294-2541dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576220 | |||||||
| chr3:139576265 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.294-2585G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576265 | |||||||
| chr3:139576296 | G | A | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
240 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.293+2576C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576296 | |||||||
| chr3:139576304 | A | C | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.293+2568T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576304 | |||||||
| chr3:139576512 | TATTAAGT others(1): Show |
T | 69 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(66): Show |
70 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(67): Show |
intron_variant | MODIFIER | c.293+2352_293+2359d others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576512 | |||||||
| chr3:139576529 | A | G | 6 | a0001c0001t0001g0212 a0001c0001t0001g0253 a0001c0001t0001g0304 others(3): Show |
6 | NA18612.hp1 NA18946.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.293+2343T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576529 | |||||||
| chr3:139576653 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293+2219G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576653 | |||||||
| chr3:139576712 | C | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+2160G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576712 | |||||||
| chr3:139576750 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.293+2122T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576750 | |||||||
| chr3:139576777 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293+2095G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576777 | |||||||
| chr3:139576885 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.293+1987C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139576885 | |||||||
| chr3:139577099 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.293+1773T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577099 | |||||||
| chr3:139577110 | T | C | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+1762A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577110 | |||||||
| chr3:139577124 | T | TC | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.293+1747dupG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577124 | |||||||
| chr3:139577125 | C | CA | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
97 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.293+1746dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577125 | |||||||
| chr3:139577371 | C | T | 5 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(2): Show |
5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+1501G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577371 | |||||||
| chr3:139577381 | G | C | 2 | a0001c0001t0001g0225 a0001c0001t0002g0055 |
2 | NA18959.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.293+1491C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577381 | |||||||
| chr3:139577849 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293+1023T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577849 | |||||||
| chr3:139577870 | A | T | 79 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.293+1002T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577870 | |||||||
| chr3:139577936 | T | C | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.293+936A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139577936 | |||||||
| chr3:139578001 | T | TG | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0167 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.293+870dupC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578001 | |||||||
| chr3:139578389 | C | A | 5 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(2): Show |
5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.293+483G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578389 | |||||||
| chr3:139578722 | CT | C | 14 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.293+149delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578722 | |||||||
| chr3:139578800 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0219 |
2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.293+72G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578800 | |||||||
| chr3:139578813 | A | G | 165 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(162): Show |
172 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.293+59T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578813 | |||||||
| chr3:139578838 | C | T | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.293+34G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578838 | |||||||
| chr3:139578851 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293+21G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 5/6 | chr3 | 139578851 | |||||||
| chr3:139579146 | G | T | 5 | a0001c0001t0001g0214 a0001c0001t0001g0267 a0001c0001t0001g0273 others(2): Show |
5 | NA18941.hp1 NA18978.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.110-91C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579146 | |||||||
| chr3:139579269 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0002g0023 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-214G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579269 | |||||||
| chr3:139579357 | C | T | 149 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
155 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.110-302G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579357 | |||||||
| chr3:139579519 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-464C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579519 | |||||||
| chr3:139579704 | G | T | 11 | a0001c0001t0001g0193 a0001c0001t0002g0041 a0001c0001t0002g0057 others(8): Show |
12 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-649C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579704 | |||||||
| chr3:139579725 | T | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
85 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.110-670A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579725 | |||||||
| chr3:139579804 | T | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(69): Show |
73 | HG00438.hp1 HG00735.hp2 HG01099.hp2 others(70): Show |
intron_variant | MODIFIER | c.110-749A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579804 | |||||||
| chr3:139579836 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.110-781T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579836 | |||||||
| chr3:139579908 | T | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-853A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139579908 | |||||||
| chr3:139580036 | G | A | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-981C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580036 | |||||||
| chr3:139580236 | T | TCTCAGCT others(41): Show |
13 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0193 others(10): Show |
14 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-1182_110-1181i others(50): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580236 | |||||||
| chr3:139580284 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.110-1229C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580284 | |||||||
| chr3:139580386 | G | T | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-1331C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580386 | |||||||
| chr3:139580425 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-1370T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580425 | |||||||
| chr3:139580814 | C | CT | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
84 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.110-1760dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580814 | |||||||
| chr3:139580958 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.110-1903G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139580958 | |||||||
| chr3:139581078 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.110-2023T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581078 | |||||||
| chr3:139581172 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-2117G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581172 | |||||||
| chr3:139581303 | A | ATAT | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.110-2251_110-2249d others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581303 | |||||||
| chr3:139581369 | C | CT | 16 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(13): Show |
18 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.110-2315dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | |||||||
| chr3:139581369 | CT | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0105 others(42): Show |
47 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.110-2315delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | |||||||
| chr3:139581369 | CTT | C | 6 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0194 others(3): Show |
7 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-2316_110-2315d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581369 | |||||||
| chr3:139581378 | T | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-2323A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581378 | |||||||
| chr3:139581647 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-2592A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581647 | |||||||
| chr3:139581717 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.110-2662A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581717 | |||||||
| chr3:139581926 | GGCTCATG others(440): Show |
G | 1 | a0001c0001t0004g0095 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.110-3318_110-2872d others(2): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581926 | |||||||
| chr3:139581939 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-2884T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139581939 | |||||||
| chr3:139582085 | C | T | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-3030G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582085 | |||||||
| chr3:139582093 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-3038C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582093 | |||||||
| chr3:139582171 | A | G | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-3116T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582171 | |||||||
| chr3:139582190 | C | CA | 25 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0104 others(22): Show |
25 | HG01074.hp2 HG01175.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.110-3136dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | |||||||
| chr3:139582190 | CA | C | 18 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0116 others(15): Show |
18 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-3136delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | |||||||
| chr3:139582190 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.110-3151_110-3136d others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582190 | |||||||
| chr3:139582206 | A | G | 12 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(9): Show |
13 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-3151T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582206 | |||||||
| chr3:139582214 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.110-3159T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582214 | |||||||
| chr3:139582215 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0214 |
2 | HG04199.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.110-3160C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582215 | |||||||
| chr3:139582216 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-3161T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582216 | |||||||
| chr3:139582336 | T | G | 80 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-3281A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582336 | |||||||
| chr3:139582639 | C | CA | 230 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.110-3585dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | |||||||
| chr3:139582639 | C | CAA | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0104 others(18): Show |
21 | HG00423.hp1 HG00621.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-3586_110-3585d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | |||||||
| chr3:139582639 | CA | C | 14 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0274 others(11): Show |
14 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-3585delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | |||||||
| chr3:139582639 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-3595_110-3585d others(13): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582639 | |||||||
| chr3:139582907 | A | T | 13 | a0001c0001t0001g0274 a0001c0001t0001g0296 a0001c0001t0002g0013 others(10): Show |
13 | HG00738.hp1 HG01081.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.110-3852T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582907 | |||||||
| chr3:139582909 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-3854A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582909 | |||||||
| chr3:139582939 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.110-3884G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582939 | |||||||
| chr3:139582956 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.110-3901A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139582956 | |||||||
| chr3:139583034 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-3979G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583034 | |||||||
| chr3:139583315 | A | G | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-4260T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583315 | |||||||
| chr3:139583415 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.110-4360A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583415 | |||||||
| chr3:139583495 | T | TTCTGAAG others(138): Show |
79 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.110-4585_110-4441d others(147): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583495 | |||||||
| chr3:139583495 | TTCTGAAG others(138): Show |
T | 9 | a0001c0001t0001g0279 a0001c0002t0001g0120 a0001c0002t0001g0122 others(6): Show |
10 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-4585_110-4441d others(2): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583495 | |||||||
| chr3:139583634 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.110-4579G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139583634 | |||||||
| chr3:139584083 | CA | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0173 a0001c0001t0001g0198 others(6): Show |
9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-5029delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584083 | |||||||
| chr3:139584235 | G | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-5180C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584235 | |||||||
| chr3:139584248 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-5193T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584248 | |||||||
| chr3:139584286 | C | T | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-5231G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584286 | |||||||
| chr3:139584343 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-5288G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584343 | |||||||
| chr3:139584406 | G | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.110-5351C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584406 | |||||||
| chr3:139584789 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-5734T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584789 | |||||||
| chr3:139584902 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-5847C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584902 | |||||||
| chr3:139584914 | C | T | 1 | a0001c0007t0001g0262 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.110-5859G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139584914 | |||||||
| chr3:139585045 | T | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-5990A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585045 | |||||||
| chr3:139585098 | C | T | 80 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-6043G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585098 | |||||||
| chr3:139585143 | C | T | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-6088G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585143 | |||||||
| chr3:139585413 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.110-6358G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585413 | |||||||
| chr3:139585531 | A | G | 1 | a0001c0004t0001g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.110-6476T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585531 | |||||||
| chr3:139585541 | G | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(73): Show |
81 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.110-6486C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585541 | |||||||
| chr3:139585996 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-6941G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139585996 | |||||||
| chr3:139586160 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.110-7105A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586160 | |||||||
| chr3:139586227 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0264 |
2 | HG00323.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.110-7172C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586227 | |||||||
| chr3:139586271 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110-7216G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586271 | |||||||
| chr3:139586443 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.110-7388A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586443 | |||||||
| chr3:139586492 | T | A | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-7437A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586492 | |||||||
| chr3:139586662 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.110-7607G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586662 | |||||||
| chr3:139586702 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | NA18993.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.110-7647C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586702 | |||||||
| chr3:139586755 | G | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-7700C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139586755 | |||||||
| chr3:139587054 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-7999C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587054 | |||||||
| chr3:139587266 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-8211C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587266 | |||||||
| chr3:139587322 | G | A | 9 | a0001c0001t0001g0125 a0001c0001t0001g0186 a0001c0001t0001g0193 others(6): Show |
10 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-8267C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587322 | |||||||
| chr3:139587345 | T | G | 9 | a0001c0001t0001g0125 a0001c0001t0001g0186 a0001c0001t0001g0193 others(6): Show |
10 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-8290A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587345 | |||||||
| chr3:139587425 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.110-8370G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587425 | |||||||
| chr3:139587442 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-8387G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587442 | |||||||
| chr3:139587470 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.110-8415G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587470 | |||||||
| chr3:139587649 | A | G | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-8594T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587649 | |||||||
| chr3:139587650 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-8595G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587650 | |||||||
| chr3:139587733 | A | C | 83 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(80): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.110-8678T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587733 | |||||||
| chr3:139587786 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.110-8731C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587786 | |||||||
| chr3:139587986 | A | G | 256 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(253): Show |
264 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.110-8931T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139587986 | |||||||
| chr3:139588058 | T | G | 1 | a0001c0001t0001g0289 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.110-9003A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588058 | |||||||
| chr3:139588318 | G | A | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-9263C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588318 | |||||||
| chr3:139588369 | G | A | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-9314C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588369 | |||||||
| chr3:139588488 | T | G | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.110-9433A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588488 | |||||||
| chr3:139588533 | G | T | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-9478C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588533 | |||||||
| chr3:139588619 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-9564G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588619 | |||||||
| chr3:139588633 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9578C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588633 | |||||||
| chr3:139588707 | T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9652A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588707 | |||||||
| chr3:139588717 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-9662G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588717 | |||||||
| chr3:139588744 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0002g0080 |
2 | NA18957.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.110-9689G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588744 | |||||||
| chr3:139588820 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-9765T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588820 | |||||||
| chr3:139588880 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-9825C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139588880 | |||||||
| chr3:139589275 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
83 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.110-10220T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589275 | |||||||
| chr3:139589305 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-10250C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589305 | |||||||
| chr3:139589477 | T | C | 7 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0057 others(4): Show |
8 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-10422A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589477 | |||||||
| chr3:139589571 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.110-10516G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589571 | |||||||
| chr3:139589808 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-10753A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589808 | |||||||
| chr3:139589904 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-10849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589904 | |||||||
| chr3:139589991 | C | T | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-10936G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139589991 | |||||||
| chr3:139590036 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0050 |
2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.110-10981C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590036 | |||||||
| chr3:139590111 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-11056G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590111 | |||||||
| chr3:139590219 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.110-11164T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590219 | |||||||
| chr3:139590449 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-11394C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590449 | |||||||
| chr3:139590692 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.110-11637C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590692 | |||||||
| chr3:139590982 | G | GGAACAGC others(6): Show |
3 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0200 |
3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11928_110-1192 others(17): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139590982 | |||||||
| chr3:139591009 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0200 |
3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11954A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591009 | |||||||
| chr3:139591011 | A | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0200 |
3 | HG02559.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.110-11956T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591011 | |||||||
| chr3:139591019 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.110-11964T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591019 | |||||||
| chr3:139591059 | G | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-12004C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591059 | |||||||
| chr3:139591091 | G | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12036C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591091 | |||||||
| chr3:139591281 | G | C | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12226C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591281 | |||||||
| chr3:139591316 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110-12261G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591316 | |||||||
| chr3:139591320 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.110-12265C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591320 | |||||||
| chr3:139591387 | C | T | 1 | a0001c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-12332G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591387 | |||||||
| chr3:139591419 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12364G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591419 | |||||||
| chr3:139591441 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-12386C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591441 | |||||||
| chr3:139591448 | G | C | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
159 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.110-12393C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591448 | |||||||
| chr3:139591604 | C | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-12549G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591604 | |||||||
| chr3:139591608 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.110-12553C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591608 | |||||||
| chr3:139591627 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0005g0009 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-12572G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591627 | |||||||
| chr3:139591644 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-12589A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591644 | |||||||
| chr3:139591696 | C | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
64 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.110-12641G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591696 | |||||||
| chr3:139591708 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0311 |
2 | NA18906.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.110-12653C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591708 | |||||||
| chr3:139591723 | A | C | 1 | a0001c0001t0001g0311 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.110-12668T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591723 | |||||||
| chr3:139591727 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.110-12672G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591727 | |||||||
| chr3:139591741 | G | C | 7 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0057 others(4): Show |
8 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.110-12686C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591741 | |||||||
| chr3:139591801 | C | T | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12746G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591801 | |||||||
| chr3:139591826 | C | A | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-12771G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591826 | |||||||
| chr3:139591866 | G | A | 83 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(80): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.110-12811C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591866 | |||||||
| chr3:139591902 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12847T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591902 | |||||||
| chr3:139591903 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.110-12848A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591903 | |||||||
| chr3:139591909 | C | T | 1 | a0001c0004t0001g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110-12854G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591909 | |||||||
| chr3:139591932 | G | A | 10 | a0001c0001t0001g0127 a0001c0001t0001g0173 a0001c0001t0001g0198 others(7): Show |
10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-12877C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139591932 | |||||||
| chr3:139592058 | T | C | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-13003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592058 | |||||||
| chr3:139592152 | T | A | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-13097A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592152 | |||||||
| chr3:139592154 | G | C | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-13099C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592154 | |||||||
| chr3:139592201 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.110-13146C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592201 | |||||||
| chr3:139592248 | G | C | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-13193C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592248 | |||||||
| chr3:139592290 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-13235C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592290 | |||||||
| chr3:139592363 | G | T | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-13308C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592363 | |||||||
| chr3:139592470 | T | G | 2 | a0001c0001t0001g0239 a0001c0001t0002g0027 |
2 | HG01106.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.110-13415A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592470 | |||||||
| chr3:139592591 | G | A | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-13536C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592591 | |||||||
| chr3:139592729 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-13674T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592729 | |||||||
| chr3:139592915 | C | T | 70 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(67): Show |
71 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-13860G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139592915 | |||||||
| chr3:139593081 | T | C | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14026A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593081 | |||||||
| chr3:139593083 | T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14028A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593083 | |||||||
| chr3:139593112 | A | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-14057T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593112 | |||||||
| chr3:139593402 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0002g0014 |
2 | HG02486.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.110-14347G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593402 | |||||||
| chr3:139593448 | G | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-14393C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593448 | |||||||
| chr3:139593457 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-14402C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593457 | |||||||
| chr3:139593531 | C | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-14476G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593531 | |||||||
| chr3:139593532 | C | T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-14477G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593532 | |||||||
| chr3:139593582 | G | GTAAAATA others(38): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0219 |
2 | HG02015.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.110-14572_110-1452 others(49): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593582 | |||||||
| chr3:139593609 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-14554T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593609 | |||||||
| chr3:139593622 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.110-14567G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593622 | |||||||
| chr3:139593655 | T | G | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-14600A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593655 | |||||||
| chr3:139593763 | T | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(67): Show |
71 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(68): Show |
intron_variant | MODIFIER | c.110-14708A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593763 | |||||||
| chr3:139593800 | A | G | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-14745T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593800 | |||||||
| chr3:139593843 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.110-14788G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593843 | |||||||
| chr3:139593852 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.110-14797C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139593852 | |||||||
| chr3:139594038 | A | G | 10 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0021 others(7): Show |
11 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-14983T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594038 | |||||||
| chr3:139594058 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0002g0050 |
2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.110-15003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594058 | |||||||
| chr3:139594106 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-15051C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594106 | |||||||
| chr3:139594150 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.110-15095T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594150 | |||||||
| chr3:139594175 | T | A | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-15120A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594175 | |||||||
| chr3:139594333 | C | T | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.110-15278G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594333 | |||||||
| chr3:139594364 | C | G | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15309G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594364 | |||||||
| chr3:139594366 | T | C | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15311A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594366 | |||||||
| chr3:139594396 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.110-15341G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594396 | |||||||
| chr3:139594492 | T | C | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15437A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594492 | |||||||
| chr3:139594494 | A | G | 8 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-15439T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594494 | |||||||
| chr3:139594537 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-15482C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594537 | |||||||
| chr3:139594570 | A | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0005g0009 |
3 | HG02723.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-15515T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594570 | |||||||
| chr3:139594580 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-15525G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594580 | |||||||
| chr3:139594581 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-15526C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594581 | |||||||
| chr3:139594688 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.110-15633T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594688 | |||||||
| chr3:139594697 | A | G | 6 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0001g0236 others(3): Show |
6 | HG00423.hp2 NA18941.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-15642T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594697 | |||||||
| chr3:139594726 | A | C | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-15671T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594726 | |||||||
| chr3:139594779 | T | G | 14 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
15 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-15724A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594779 | |||||||
| chr3:139594849 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0186 a0001c0001t0001g0193 others(2): Show |
5 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-15794C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594849 | |||||||
| chr3:139594957 | G | T | 1 | a0001c0001t0002g0075 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.110-15902C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594957 | |||||||
| chr3:139594998 | A | G | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-15943T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139594998 | |||||||
| chr3:139595037 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.110-15982G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595037 | |||||||
| chr3:139595099 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.110-16044T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595099 | |||||||
| chr3:139595369 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-16314C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595369 | |||||||
| chr3:139595423 | G | C | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.110-16368C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595423 | |||||||
| chr3:139595492 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-16437G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595492 | |||||||
| chr3:139595493 | G | T | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-16438C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595493 | |||||||
| chr3:139595585 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.110-16530T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595585 | |||||||
| chr3:139595629 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.110-16574G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595629 | |||||||
| chr3:139595663 | T | G | 4 | a0001c0002t0001g0175 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-16608A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595663 | |||||||
| chr3:139595708 | G | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16653C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595708 | |||||||
| chr3:139595710 | A | C | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16655T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595710 | |||||||
| chr3:139595711 | A | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16656T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595711 | |||||||
| chr3:139595712 | A | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16657T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595712 | |||||||
| chr3:139595714 | G | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16659C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595714 | |||||||
| chr3:139595715 | A | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16660T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595715 | |||||||
| chr3:139595717 | TCCC | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16665_110-1666 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595717 | |||||||
| chr3:139595728 | TA | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(70): Show |
74 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(71): Show |
intron_variant | MODIFIER | c.110-16674delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595728 | |||||||
| chr3:139595887 | G | T | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-16832C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595887 | |||||||
| chr3:139595946 | C | T | 15 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(12): Show |
16 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-16891G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139595946 | |||||||
| chr3:139596136 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.110-17081G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596136 | |||||||
| chr3:139596194 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.110-17139A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596194 | |||||||
| chr3:139596204 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.110-17149C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596204 | |||||||
| chr3:139596379 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.110-17324A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596379 | |||||||
| chr3:139596397 | A | C | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-17342T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596397 | |||||||
| chr3:139596561 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-17506A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596561 | |||||||
| chr3:139596599 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
99 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.110-17544T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596599 | |||||||
| chr3:139596744 | T | C | 12 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(9): Show |
13 | HG01175.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-17689A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596744 | |||||||
| chr3:139596860 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0002g0051 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.110-17805G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596860 | |||||||
| chr3:139596896 | A | G | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-17841T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596896 | |||||||
| chr3:139596910 | A | ATG | 15 | a0001c0001t0001g0127 a0001c0001t0001g0144 a0001c0001t0001g0157 others(12): Show |
15 | HG01123.hp1 HG01516.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.110-17857_110-1785 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596910 | |||||||
| chr3:139596916 | G | GTATA | 3 | a0001c0001t0001g0105 a0001c0001t0001g0121 a0001c0004t0001g0119 |
3 | HG01109.hp1 HG02896.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.110-17865_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.110-17871_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTA | 10 | a0001c0001t0001g0137 a0001c0001t0001g0160 a0001c0001t0001g0197 others(7): Show |
10 | HG00733.hp1 HG02145.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTATA | 12 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0198 others(9): Show |
12 | HG00642.hp2 HG01106.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTATAT others(1): Show |
3 | a0001c0001t0001g0161 a0001c0001t0001g0241 a0001c0001t0001g0289 |
3 | HG03017.hp1 NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTATAT others(3): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0155 a0001c0001t0001g0246 |
3 | HG00280.hp1 HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTATAT others(7): Show |
4 | a0001c0001t0001g0166 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | HG00735.hp1 HG01515.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17862_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTATAT others(9): Show |
1 | a0001c0001t0001g0231 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.110-17862_110-1786 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | G | GTGTGTAT others(7): Show |
2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.110-17862_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTA | G | 10 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(7): Show |
10 | HG01069.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-17863_110-1786 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATA | G | 13 | a0001c0001t0001g0097 a0001c0001t0001g0117 a0001c0001t0001g0132 others(10): Show |
13 | HG00423.hp1 HG00621.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.110-17865_110-1786 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATA | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0296 a0001c0004t0001g0147 others(1): Show |
4 | HG00735.hp2 HG02965.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17867_110-1786 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(3): Show |
G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0170 a0001c0001t0001g0183 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-17871_110-1786 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(5): Show |
G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0167 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.110-17873_110-1786 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(7): Show |
G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0153 a0001c0001t0001g0189 others(12): Show |
18 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-17875_110-1786 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(9): Show |
G | 18 | a0001c0001t0001g0109 a0001c0001t0001g0126 a0001c0001t0001g0171 others(15): Show |
18 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.110-17877_110-1786 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(11): Show |
G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0128 others(44): Show |
49 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.110-17879_110-1786 others(22): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(13): Show |
G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0163 a0001c0001t0001g0164 others(10): Show |
14 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.110-17881_110-1786 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(15): Show |
G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0255 a0001c0001t0001g0301 others(1): Show |
4 | HG02273.hp1 HG03486.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17883_110-1786 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(17): Show |
G | 71 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(68): Show |
72 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(69): Show |
intron_variant | MODIFIER | c.110-17885_110-1786 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-17887_110-1786 others(30): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(21): Show |
G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-17889_110-1786 others(32): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(25): Show |
G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-17893_110-1786 others(36): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(29): Show |
G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0263 a0001c0001t0002g0057 others(1): Show |
4 | HG02717.hp1 HG03942.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17897_110-1786 others(40): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(31): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-17899_110-1786 others(42): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596916 | GTATATAT others(33): Show |
G | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.110-17901_110-1786 others(44): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596916 | |||||||
| chr3:139596918 | A | G | 25 | a0001c0001t0001g0098 a0001c0001t0001g0134 a0001c0001t0001g0136 others(22): Show |
26 | HG00639.hp2 HG01175.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.110-17863T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596918 | |||||||
| chr3:139596920 | A | G | 10 | a0001c0001t0001g0138 a0001c0001t0001g0275 a0001c0002t0001g0120 others(7): Show |
11 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-17865T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596920 | |||||||
| chr3:139596922 | A | G | 15 | a0001c0001t0001g0097 a0001c0001t0001g0132 a0001c0001t0001g0216 others(12): Show |
16 | HG00423.hp1 HG00621.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-17867T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596922 | |||||||
| chr3:139596926 | A | G | 2 | a0001c0001t0001g0251 a0001c0001t0002g0070 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.110-17871T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596926 | |||||||
| chr3:139596928 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0264 |
2 | HG00323.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.110-17873T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596928 | |||||||
| chr3:139596930 | A | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0314 |
2 | HG01081.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.110-17875T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596930 | |||||||
| chr3:139596932 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0153 a0001c0001t0001g0189 others(12): Show |
18 | HG01515.hp2 HG01517.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.110-17877T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596932 | |||||||
| chr3:139596934 | A | G | 17 | a0001c0001t0001g0109 a0001c0001t0001g0126 a0001c0001t0001g0171 others(14): Show |
17 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-17879T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596934 | |||||||
| chr3:139596936 | A | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0128 others(44): Show |
49 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.110-17881T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596936 | |||||||
| chr3:139596938 | A | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0077 |
2 | HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.110-17883T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596938 | |||||||
| chr3:139596939 | TATATATA others(10): Show |
T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17901_110-1788 others(21): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596939 | |||||||
| chr3:139596940 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0255 a0001c0001t0001g0301 others(1): Show |
4 | HG02273.hp1 HG03486.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17885T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596940 | |||||||
| chr3:139596942 | A | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(69): Show |
73 | HG00438.hp1 HG01099.hp2 HG01192.hp1 others(70): Show |
intron_variant | MODIFIER | c.110-17887T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596942 | |||||||
| chr3:139596943 | TATATATA others(8): Show |
T | 5 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(2): Show |
5 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-17903_110-1788 others(19): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596943 | |||||||
| chr3:139596954 | A | G | 2 | a0001c0001t0001g0263 a0003c0006t0001g0261 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.110-17899T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596954 | |||||||
| chr3:139596956 | ATATATAT others(3): Show |
A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-17911_110-1790 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596956 | |||||||
| chr3:139596958 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.110-17903T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596958 | |||||||
| chr3:139596958 | A | T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-17903T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596958 | |||||||
| chr3:139596960 | A | T | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-17905T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596960 | |||||||
| chr3:139596962 | A | T | 11 | a0001c0001t0001g0188 a0001c0001t0002g0002 a0001c0001t0002g0003 others(8): Show |
14 | HG01175.hp1 HG01496.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-17907T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596962 | |||||||
| chr3:139596964 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.110-17910_110-1790 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596964 | |||||||
| chr3:139596964 | A | T | 23 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(20): Show |
26 | HG00280.hp1 HG00733.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.110-17909T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139596964 | |||||||
| chr3:139597027 | G | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-17972C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597027 | |||||||
| chr3:139597167 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.110-18112G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597167 | |||||||
| chr3:139597197 | T | C | 84 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-18142A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597197 | |||||||
| chr3:139597367 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-18312A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597367 | |||||||
| chr3:139597375 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-18320C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597375 | |||||||
| chr3:139597533 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-18478G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597533 | |||||||
| chr3:139597565 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.110-18510C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597565 | |||||||
| chr3:139597584 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-18529T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597584 | |||||||
| chr3:139597940 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-18885T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597940 | |||||||
| chr3:139597972 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0230 |
2 | HG01243.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.110-18917C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139597972 | |||||||
| chr3:139598072 | A | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0041 others(1): Show |
4 | HG01243.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.110-19017T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598072 | |||||||
| chr3:139598164 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.110-19109C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598164 | |||||||
| chr3:139598367 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-19312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598367 | |||||||
| chr3:139598377 | T | C | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.110-19322A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598377 | |||||||
| chr3:139598392 | T | C | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-19337A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598392 | |||||||
| chr3:139598863 | T | C | 8 | a0001c0002t0001g0120 a0001c0002t0001g0122 a0001c0002t0001g0123 others(5): Show |
9 | HG01175.hp1 HG01496.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.110-19808A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139598863 | |||||||
| chr3:139599131 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-20076T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599131 | |||||||
| chr3:139599252 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0002g0057 |
3 | HG01243.hp2 HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.110-20197G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599252 | |||||||
| chr3:139599399 | A | T | 84 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-20344T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599399 | |||||||
| chr3:139599626 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.110-20571G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599626 | |||||||
| chr3:139599818 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.110-20763G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139599818 | |||||||
| chr3:139600131 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.110-21076T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600131 | |||||||
| chr3:139600182 | T | C | 1 | a0001c0001t0005g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.110-21127A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600182 | |||||||
| chr3:139600306 | A | AT | 42 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0105 others(39): Show |
44 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.110-21252dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600306 | |||||||
| chr3:139600430 | C | T | 82 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.110-21375G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600430 | |||||||
| chr3:139600518 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.110-21463C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600518 | |||||||
| chr3:139600633 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-21578G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600633 | |||||||
| chr3:139600793 | C | G | 9 | a0001c0001t0001g0008 a0001c0001t0001g0272 a0001c0001t0001g0290 others(6): Show |
10 | HG01192.hp1 HG02165.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-21738G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139600793 | |||||||
| chr3:139601155 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-22100A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601155 | |||||||
| chr3:139601248 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.110-22193C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601248 | |||||||
| chr3:139601760 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.110-22705A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601760 | |||||||
| chr3:139601795 | G | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
156 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.110-22740C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139601795 | |||||||
| chr3:139602080 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0196 |
2 | HG01256.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.110-23025G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602080 | |||||||
| chr3:139602165 | A | T | 2 | a0001c0001t0001g0185 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.110-23110T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602165 | |||||||
| chr3:139602392 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.110-23337T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602392 | |||||||
| chr3:139602710 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-23655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602710 | |||||||
| chr3:139602820 | T | C | 17 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(14): Show |
17 | HG01099.hp2 HG01433.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.110-23765A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602820 | |||||||
| chr3:139602887 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.110-23832G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139602887 | |||||||
| chr3:139603264 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.110-24209G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603264 | |||||||
| chr3:139603266 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.110-24211A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603266 | |||||||
| chr3:139603280 | G | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-24225C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603280 | |||||||
| chr3:139603305 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.110-24250A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603305 | |||||||
| chr3:139603506 | C | G | 250 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(247): Show |
257 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.109+24110G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603506 | |||||||
| chr3:139603524 | CA | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0163 a0001c0001t0001g0164 others(10): Show |
14 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+24091delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603524 | |||||||
| chr3:139603613 | ACCG | A | 18 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 others(15): Show |
18 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.109+24000_109+2400 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603613 | |||||||
| chr3:139603616 | G | A | 12 | a0001c0001t0001g0125 a0001c0001t0001g0163 a0001c0001t0001g0164 others(9): Show |
13 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+24000C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603616 | |||||||
| chr3:139603625 | G | A | 97 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0125 others(94): Show |
99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.109+23991C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603625 | |||||||
| chr3:139603642 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0002g0057 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109+23974C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603642 | |||||||
| chr3:139603743 | A | C | 66 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0106 others(63): Show |
66 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.109+23873T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603743 | |||||||
| chr3:139603805 | AC | A | 17 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0109 others(14): Show |
17 | HG01123.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+23810delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139603805 | |||||||
| chr3:139604032 | G | T | 21 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0121 others(18): Show |
21 | HG01123.hp1 HG01175.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.109+23584C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604032 | |||||||
| chr3:139604118 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+23498G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604118 | |||||||
| chr3:139604206 | C | G | 1 | a0001c0007t0001g0262 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.109+23410G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604206 | |||||||
| chr3:139604310 | A | C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0179 others(4): Show |
7 | HG01123.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+23306T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604310 | |||||||
| chr3:139604476 | T | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+23140A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604476 | |||||||
| chr3:139604521 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.109+23095C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604521 | |||||||
| chr3:139604672 | A | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0050 |
4 | HG01257.hp1 HG01258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+22944T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604672 | |||||||
| chr3:139604739 | T | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+22877A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604739 | |||||||
| chr3:139604818 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0210 |
2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.109+22798A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604818 | |||||||
| chr3:139604839 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.109+22777A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604839 | |||||||
| chr3:139604910 | G | A | 80 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0098 others(77): Show |
81 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.109+22706C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139604910 | |||||||
| chr3:139605040 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+22576T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605040 | |||||||
| chr3:139605043 | AC | A | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+22572delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605043 | |||||||
| chr3:139605073 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+22543C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605073 | |||||||
| chr3:139605149 | G | C | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.109+22467C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605149 | |||||||
| chr3:139605617 | C | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.109+21999G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605617 | |||||||
| chr3:139605771 | T | G | 30 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(27): Show |
30 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.109+21845A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605771 | |||||||
| chr3:139605914 | AT | A | 50 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0129 others(47): Show |
50 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.109+21701delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | |||||||
| chr3:139605914 | ATT | A | 251 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(248): Show |
258 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.109+21700_109+2170 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | |||||||
| chr3:139605914 | ATTT | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0137 a0001c0001t0001g0143 others(3): Show |
7 | HG01256.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+21699_109+2170 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605914 | |||||||
| chr3:139605995 | A | G | 77 | a0001c0001t0001g0008 a0001c0001t0001g0097 a0001c0001t0001g0098 others(74): Show |
78 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.109+21621T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139605995 | |||||||
| chr3:139606162 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+21454G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606162 | |||||||
| chr3:139606187 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.109+21429T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606187 | |||||||
| chr3:139606258 | C | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0156 others(3): Show |
6 | HG02015.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+21358G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606258 | |||||||
| chr3:139606514 | G | C | 17 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(14): Show |
17 | HG01243.hp1 HG01433.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.109+21102C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606514 | |||||||
| chr3:139606642 | A | G | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.109+20974T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606642 | |||||||
| chr3:139606903 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+20713C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606903 | |||||||
| chr3:139606990 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+20626G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139606990 | |||||||
| chr3:139607215 | T | C | 262 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
270 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.109+20401A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607215 | |||||||
| chr3:139607310 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+20306G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607310 | |||||||
| chr3:139607642 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
141 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.109+19974A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607642 | |||||||
| chr3:139607663 | G | GT | 289 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(286): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.109+19952dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607663 | |||||||
| chr3:139607684 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+19932A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139607684 | |||||||
| chr3:139608024 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.109+19592T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608024 | |||||||
| chr3:139608176 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.109+19440G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608176 | |||||||
| chr3:139608332 | TAACA | T | 274 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(271): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.109+19280_109+1928 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608332 | |||||||
| chr3:139608419 | A | G | 207 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.109+19197T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608419 | |||||||
| chr3:139608494 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.109+19122G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608494 | |||||||
| chr3:139608882 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0031 a0001c0001t0002g0032 |
3 | HG00639.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.109+18734G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608882 | |||||||
| chr3:139608895 | G | C | 278 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(275): Show |
286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.109+18721C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139608895 | |||||||
| chr3:139609130 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+18486G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609130 | |||||||
| chr3:139609385 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+18231G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609385 | |||||||
| chr3:139609538 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(44): Show |
48 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.109+18078G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609538 | |||||||
| chr3:139609546 | G | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+18070C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609546 | |||||||
| chr3:139609563 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+18053C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609563 | |||||||
| chr3:139609582 | T | TTTAA | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+18033_109+1803 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609582 | |||||||
| chr3:139609633 | G | A | 18 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(15): Show |
18 | HG01433.hp2 HG02602.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.109+17983C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609633 | |||||||
| chr3:139609657 | G | GT | 187 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.109+17958dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609657 | |||||||
| chr3:139609667 | T | TC | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
98 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.109+17948_109+1794 others(5): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609667 | |||||||
| chr3:139609872 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.109+17744T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609872 | |||||||
| chr3:139609892 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+17724A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609892 | |||||||
| chr3:139609897 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+17719G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139609897 | |||||||
| chr3:139610001 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.109+17615A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610001 | |||||||
| chr3:139610070 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+17546C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610070 | |||||||
| chr3:139610499 | A | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+17117T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610499 | |||||||
| chr3:139610509 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+17107G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610509 | |||||||
| chr3:139610606 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+17010T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610606 | |||||||
| chr3:139610738 | T | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16878A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610738 | |||||||
| chr3:139610764 | T | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16852A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610764 | |||||||
| chr3:139610773 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109+16843T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610773 | |||||||
| chr3:139610821 | C | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16795G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610821 | |||||||
| chr3:139610844 | C | T | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+16772G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139610844 | |||||||
| chr3:139611035 | TGGG | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16578_109+1658 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611035 | |||||||
| chr3:139611047 | T | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16569A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611047 | |||||||
| chr3:139611096 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+16520A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611096 | |||||||
| chr3:139611137 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.109+16479G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611137 | |||||||
| chr3:139611194 | T | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+16422A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611194 | |||||||
| chr3:139611517 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+16099A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611517 | |||||||
| chr3:139611561 | T | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.109+16055A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611561 | |||||||
| chr3:139611753 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15863T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611753 | |||||||
| chr3:139611761 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(44): Show |
48 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.109+15855G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611761 | |||||||
| chr3:139611762 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.109+15854C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611762 | |||||||
| chr3:139611785 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+15831T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611785 | |||||||
| chr3:139611817 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15799T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611817 | |||||||
| chr3:139611851 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0002g0051 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+15765A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611851 | |||||||
| chr3:139611884 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15732C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611884 | |||||||
| chr3:139611899 | T | G | 284 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(281): Show |
292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.109+15717A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611899 | |||||||
| chr3:139611951 | G | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15665C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611951 | |||||||
| chr3:139611958 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+15658C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611958 | |||||||
| chr3:139611974 | C | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15642G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139611974 | |||||||
| chr3:139612036 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15580C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612036 | |||||||
| chr3:139612102 | A | G | 281 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(278): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.109+15514T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612102 | |||||||
| chr3:139612120 | CTG | C | 13 | a0001c0001t0001g0215 a0001c0001t0001g0237 a0001c0001t0001g0296 others(10): Show |
13 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+15494_109+1549 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612120 | |||||||
| chr3:139612135 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+15481G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612135 | |||||||
| chr3:139612167 | C | CA | 151 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(148): Show |
153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.109+15448dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | |||||||
| chr3:139612167 | C | CAA | 8 | a0001c0001t0001g0124 a0001c0001t0001g0164 a0001c0001t0001g0167 others(5): Show |
8 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+15447_109+1544 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | |||||||
| chr3:139612167 | CA | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
75 | HG00423.hp2 HG00438.hp2 HG01099.hp2 others(72): Show |
intron_variant | MODIFIER | c.109+15448delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612167 | |||||||
| chr3:139612219 | G | A | 117 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(114): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+15397C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612219 | |||||||
| chr3:139612255 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+15361C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612255 | |||||||
| chr3:139612384 | T | C | 1 | a0001c0001t0012g0238 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.109+15232A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612384 | |||||||
| chr3:139612452 | T | G | 283 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.109+15164A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612452 | |||||||
| chr3:139612550 | T | C | 283 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.109+15066A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612550 | |||||||
| chr3:139612618 | A | C | 4 | a0001c0001t0001g0105 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
4 | HG01099.hp2 HG01109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+14998T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612618 | |||||||
| chr3:139612803 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+14813T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612803 | |||||||
| chr3:139612999 | A | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0257 |
2 | NA18941.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.109+14617T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139612999 | |||||||
| chr3:139613120 | A | C | 285 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
293 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.109+14496T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613120 | |||||||
| chr3:139613139 | C | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14477G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613139 | |||||||
| chr3:139613193 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14423C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613193 | |||||||
| chr3:139613205 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14411C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613205 | |||||||
| chr3:139613206 | A | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14410T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613206 | |||||||
| chr3:139613213 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14403A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613213 | |||||||
| chr3:139613222 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14394A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613222 | |||||||
| chr3:139613227 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.109+14389A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613227 | |||||||
| chr3:139613253 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14363G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613253 | |||||||
| chr3:139613256 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14360C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613256 | |||||||
| chr3:139613356 | T | C | 11 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+14260A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613356 | |||||||
| chr3:139613411 | A | C | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.109+14205T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613411 | |||||||
| chr3:139613448 | C | G | 1 | a0001c0001t0002g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.109+14168G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613448 | |||||||
| chr3:139613456 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14160C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613456 | |||||||
| chr3:139613506 | G | A | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+14110C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613506 | |||||||
| chr3:139613514 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+14102G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613514 | |||||||
| chr3:139613529 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.109+14087A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613529 | |||||||
| chr3:139613542 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.109+14074C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613542 | |||||||
| chr3:139613592 | C | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+14024G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613592 | |||||||
| chr3:139613642 | C | T | 117 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(114): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+13974G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613642 | |||||||
| chr3:139613675 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0237 a0001c0001t0001g0296 |
3 | NA18961.hp1 NA19065.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.109+13941G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613675 | |||||||
| chr3:139613725 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+13891C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613725 | |||||||
| chr3:139613785 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0287 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+13831G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613785 | |||||||
| chr3:139613867 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109+13749G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613867 | |||||||
| chr3:139613903 | C | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+13713G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613903 | |||||||
| chr3:139613946 | A | G | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+13670T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613946 | |||||||
| chr3:139613961 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109+13655C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139613961 | |||||||
| chr3:139614001 | G | C | 2 | a0001c0001t0001g0117 a0001c0001t0006g0044 |
2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.109+13615C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614001 | |||||||
| chr3:139614003 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+13613C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614003 | |||||||
| chr3:139614042 | C | G | 9 | a0001c0001t0001g0173 a0001c0001t0001g0204 a0001c0001t0001g0205 others(6): Show |
9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+13574G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614042 | |||||||
| chr3:139614224 | C | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+13392G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614224 | |||||||
| chr3:139614241 | T | TA | 5 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0199 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+13374dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614241 | |||||||
| chr3:139614256 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+13360G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614256 | |||||||
| chr3:139614539 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+13077G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614539 | |||||||
| chr3:139614654 | T | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12962A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614654 | |||||||
| chr3:139614671 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+12945C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614671 | |||||||
| chr3:139614768 | G | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+12848C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614768 | |||||||
| chr3:139614823 | G | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12793C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614823 | |||||||
| chr3:139614961 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+12655A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139614961 | |||||||
| chr3:139615081 | C | G | 16 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01433.hp2 HG02615.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.109+12535G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615081 | |||||||
| chr3:139615189 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.109+12427G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615189 | |||||||
| chr3:139615415 | T | TTCTATCT others(3): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0208 |
2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.109+12200_109+1220 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615415 | |||||||
| chr3:139615417 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0208 |
2 | HG02015.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.109+12199A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTA | 78 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(75): Show |
81 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.109+12195_109+1219 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(1): Show |
86 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0117 others(83): Show |
88 | HG00438.hp2 HG00621.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.109+12191_109+1219 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(5): Show |
61 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0128 others(58): Show |
63 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.109+12187_109+1219 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(9): Show |
41 | a0001c0001t0001g0106 a0001c0001t0001g0118 a0001c0001t0001g0127 others(38): Show |
42 | HG00323.hp1 HG00423.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.109+12183_109+1219 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(13): Show |
10 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0235 others(7): Show |
10 | HG00438.hp1 HG02155.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+12179_109+1219 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(17): Show |
3 | a0001c0001t0001g0160 a0001c0001t0001g0220 a0001c0001t0001g0232 |
3 | HG02080.hp2 HG02523.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.109+12175_109+1219 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615417 | T | TTCTATCT others(13): Show |
1 | a0001c0001t0001g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.109+12198_109+1219 others(24): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615417 | |||||||
| chr3:139615460 | T | TATCTATC others(9): Show |
1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+12155_109+1215 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615460 | |||||||
| chr3:139615464 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0239 |
2 | HG01243.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.109+12152G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615464 | |||||||
| chr3:139615466 | TCCAC | T | 134 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(131): Show |
136 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.109+12146_109+1214 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615466 | |||||||
| chr3:139615470 | C | T | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
152 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.109+12146G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615470 | |||||||
| chr3:139615474 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+12142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615474 | |||||||
| chr3:139615478 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+12138A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615478 | |||||||
| chr3:139615507 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+12109G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615507 | |||||||
| chr3:139615650 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0050 |
4 | HG01257.hp1 HG01258.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+11966A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615650 | |||||||
| chr3:139615724 | G | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+11892C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615724 | |||||||
| chr3:139615725 | CGTGT | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+11887_109+1189 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615725 | |||||||
| chr3:139615827 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.109+11789G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615827 | |||||||
| chr3:139615867 | TTG | T | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+11747_109+1174 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615867 | |||||||
| chr3:139615874 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+11742C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139615874 | |||||||
| chr3:139616164 | C | T | 13 | a0001c0001t0001g0127 a0001c0001t0001g0173 a0001c0001t0001g0198 others(10): Show |
13 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+11452G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616164 | |||||||
| chr3:139616268 | T | C | 13 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0179 others(10): Show |
13 | HG01123.hp1 HG01175.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.109+11348A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616268 | |||||||
| chr3:139616270 | A | T | 1 | a0001c0001t0002g0078 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.109+11346T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616270 | |||||||
| chr3:139616523 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.109+11093T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616523 | |||||||
| chr3:139616536 | A | T | 4 | a0001c0001t0001g0105 a0001c0001t0002g0011 a0001c0001t0002g0012 others(1): Show |
4 | HG01099.hp2 HG01109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+11080T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616536 | |||||||
| chr3:139616661 | T | G | 1 | a0001c0001t0001g0240 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.109+10955A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616661 | |||||||
| chr3:139616774 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0002g0041 |
2 | HG02080.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.109+10842G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616774 | |||||||
| chr3:139616776 | G | C | 1 | a0001c0001t0002g0004 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.109+10840C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616776 | |||||||
| chr3:139616806 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0290 |
2 | NA18974.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.109+10810C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616806 | |||||||
| chr3:139616821 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+10795G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616821 | |||||||
| chr3:139616851 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.109+10765A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139616851 | |||||||
| chr3:139617253 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+10363T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617253 | |||||||
| chr3:139617321 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0108 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.109+10295C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617321 | |||||||
| chr3:139617444 | C | T | 117 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(114): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+10172G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617444 | |||||||
| chr3:139617539 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109+10077A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617539 | |||||||
| chr3:139617539 | T | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
150 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.109+10077A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617539 | |||||||
| chr3:139617555 | C | T | 2 | a0001c0001t0001g0162 a0001c0004t0001g0147 |
2 | HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.109+10061G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617555 | |||||||
| chr3:139617593 | T | C | 1 | a0001c0001t0001g0007 | 2 | NA18950.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.109+10023A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617593 | |||||||
| chr3:139617902 | T | C | 40 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(37): Show |
40 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.109+9714A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139617902 | |||||||
| chr3:139618478 | G | GGAAA | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+9134_109+9137d others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618478 | |||||||
| chr3:139618770 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.109+8846T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618770 | |||||||
| chr3:139618864 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0229 |
2 | NA18971.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.109+8752T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618864 | |||||||
| chr3:139618957 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109+8659C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139618957 | |||||||
| chr3:139619285 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.109+8331C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619285 | |||||||
| chr3:139619400 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.109+8216A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619400 | |||||||
| chr3:139619781 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0002g0070 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.109+7835G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619781 | |||||||
| chr3:139619787 | A | G | 11 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+7829T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619787 | |||||||
| chr3:139619873 | T | C | 1 | a0001c0001t0009g0268 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.109+7743A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619873 | |||||||
| chr3:139619922 | A | C | 14 | a0001c0001t0001g0124 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
14 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+7694T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139619922 | |||||||
| chr3:139620028 | AT | A | 36 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.109+7587delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620028 | |||||||
| chr3:139620103 | T | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+7513A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620103 | |||||||
| chr3:139620136 | G | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
101 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(98): Show |
intron_variant | MODIFIER | c.109+7480C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620136 | |||||||
| chr3:139620156 | G | C | 1 | a0001c0001t0002g0076 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.109+7460C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620156 | |||||||
| chr3:139620200 | C | CT | 31 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(28): Show |
31 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.109+7415dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | |||||||
| chr3:139620200 | C | CTT | 41 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(38): Show |
41 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.109+7414_109+7415d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | |||||||
| chr3:139620200 | CT | C | 9 | a0001c0001t0001g0097 a0001c0001t0001g0109 a0001c0001t0001g0118 others(6): Show |
9 | HG01169.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.109+7415delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620200 | |||||||
| chr3:139620254 | C | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0180 a0001c0002t0001g0175 |
3 | HG02895.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.109+7362G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620254 | |||||||
| chr3:139620767 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+6849C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620767 | |||||||
| chr3:139620771 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+6845A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620771 | |||||||
| chr3:139620820 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.109+6796C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620820 | |||||||
| chr3:139620956 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.109+6660C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139620956 | |||||||
| chr3:139621058 | C | T | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+6558G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621058 | |||||||
| chr3:139621135 | T | G | 1 | a0001c0002t0001g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+6481A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621135 | |||||||
| chr3:139621176 | G | A | 11 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(8): Show |
11 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+6440C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621176 | |||||||
| chr3:139621294 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.109+6322A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621294 | |||||||
| chr3:139621304 | T | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(105): Show |
intron_variant | MODIFIER | c.109+6312A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621304 | |||||||
| chr3:139621305 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.109+6311A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621305 | |||||||
| chr3:139621386 | T | C | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+6230A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621386 | |||||||
| chr3:139621394 | C | T | 6 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0001c0001t0001g0190 others(3): Show |
6 | HG01433.hp2 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+6222G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621394 | |||||||
| chr3:139621612 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+6004A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621612 | |||||||
| chr3:139621876 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+5740G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621876 | |||||||
| chr3:139621972 | C | G | 1 | a0001c0001t0001g0298 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.109+5644G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139621972 | |||||||
| chr3:139622054 | G | T | 36 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.109+5562C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622054 | |||||||
| chr3:139622070 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.109+5546A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622070 | |||||||
| chr3:139622376 | AT | A | 39 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(36): Show |
39 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.109+5239delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622376 | |||||||
| chr3:139622420 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0002g0051 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+5196C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622420 | |||||||
| chr3:139622452 | ACGCCAG | A | 117 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0115 others(114): Show |
119 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.109+5158_109+5163d others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622452 | |||||||
| chr3:139622501 | G | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+5115C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622501 | |||||||
| chr3:139622576 | T | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
98 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(95): Show |
intron_variant | MODIFIER | c.109+5040A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622576 | |||||||
| chr3:139622578 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+5038G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622578 | |||||||
| chr3:139622722 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+4894T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622722 | |||||||
| chr3:139622768 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.109+4848A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622768 | |||||||
| chr3:139622771 | C | CATATATA others(4): Show |
5 | a0001c0001t0001g0117 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | HG00738.hp2 HG01106.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+4834_109+4844d others(13): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622771 | |||||||
| chr3:139622780 | G | T | 2 | a0001c0001t0001g0169 a0001c0001t0002g0051 |
2 | HG00099.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.109+4836C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622780 | |||||||
| chr3:139622817 | T | C | 2 | a0001c0001t0002g0011 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+4799A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622817 | |||||||
| chr3:139622848 | T | TTA | 61 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0001g0100 others(58): Show |
65 | HG00738.hp2 HG01106.hp1 HG01169.hp2 others(62): Show |
intron_variant | MODIFIER | c.109+4766_109+4767d others(4): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622848 | |||||||
| chr3:139622848 | T | TTATA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0126 others(44): Show |
49 | HG00423.hp2 HG00438.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.109+4764_109+4767d others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622848 | |||||||
| chr3:139622850 | A | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0200 a0001c0001t0002g0011 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+4766T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622850 | |||||||
| chr3:139622865 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0004g0095 a0001c0001t0004g0096 |
3 | HG01081.hp2 HG02293.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.109+4751A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622865 | |||||||
| chr3:139622941 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0156 a0001c0001t0001g0307 |
3 | NA18966.hp2 NA19004.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.109+4675C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622941 | |||||||
| chr3:139622962 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.109+4654G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622962 | |||||||
| chr3:139622964 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(277): Show |
288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.109+4652C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139622964 | |||||||
| chr3:139623241 | T | C | 157 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.109+4375A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623241 | |||||||
| chr3:139623335 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0185 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.109+4281C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623335 | |||||||
| chr3:139623373 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.109+4243A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623373 | |||||||
| chr3:139623486 | G | T | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+4130C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623486 | |||||||
| chr3:139623531 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.109+4085G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623531 | |||||||
| chr3:139623583 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+4033C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623583 | |||||||
| chr3:139623622 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.109+3994G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623622 | |||||||
| chr3:139623647 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+3969T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623647 | |||||||
| chr3:139623699 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+3917C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623699 | |||||||
| chr3:139623736 | C | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0296 |
2 | NA18961.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.109+3880G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623736 | |||||||
| chr3:139623745 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.109+3871C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623745 | |||||||
| chr3:139623848 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.109+3768A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623848 | |||||||
| chr3:139623969 | C | T | 159 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.109+3647G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139623969 | |||||||
| chr3:139624191 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+3425C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624191 | |||||||
| chr3:139624451 | C | CT | 8 | a0001c0001t0001g0220 a0001c0001t0001g0228 a0001c0001t0001g0235 others(5): Show |
8 | HG00423.hp2 HG02145.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+3164dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624451 | |||||||
| chr3:139624510 | C | T | 9 | a0001c0001t0001g0173 a0001c0001t0001g0204 a0001c0001t0001g0205 others(6): Show |
9 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+3106G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624510 | |||||||
| chr3:139624637 | C | T | 2 | a0001c0001t0001g0105 a0004c0008t0001g0159 |
2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.109+2979G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624637 | |||||||
| chr3:139624657 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.109+2959G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624657 | |||||||
| chr3:139624747 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.109+2869G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624747 | |||||||
| chr3:139624887 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+2729T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624887 | |||||||
| chr3:139624940 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+2676A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624940 | |||||||
| chr3:139624997 | T | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00423.hp2 HG00438.hp2 HG00738.hp2 others(107): Show |
intron_variant | MODIFIER | c.109+2619A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139624997 | |||||||
| chr3:139625799 | A | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+1817T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625799 | |||||||
| chr3:139625817 | G | A | 14 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0178 others(11): Show |
14 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+1799C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625817 | |||||||
| chr3:139625886 | C | T | 21 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0142 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.109+1730G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625886 | |||||||
| chr3:139625887 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+1729C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139625887 | |||||||
| chr3:139626012 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+1604C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626012 | |||||||
| chr3:139626029 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+1587A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626029 | |||||||
| chr3:139626193 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109+1423T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626193 | |||||||
| chr3:139626356 | C | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0041 |
2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109+1260G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626356 | |||||||
| chr3:139626361 | C | A | 156 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(153): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.109+1255G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626361 | |||||||
| chr3:139626628 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.109+988A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626628 | |||||||
| chr3:139626752 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.109+864A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626752 | |||||||
| chr3:139626766 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+850A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139626766 | |||||||
| chr3:139627155 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+461C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139627155 | |||||||
| chr3:139627572 | T | C | 1 | a0001c0001t0006g0044 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+44A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 4/6 | chr3 | 139627572 | |||||||
| chr3:139627800 | G | A | 1 | a0003c0006t0001g0261 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-40-36C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139627800 | |||||||
| chr3:139627842 | C | G | 70 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(67): Show |
71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.-40-78G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139627842 | |||||||
| chr3:139628032 | C | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0069 others(1): Show |
4 | HG00741.hp1 HG02300.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-268G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628032 | |||||||
| chr3:139628214 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-40-450A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628214 | |||||||
| chr3:139628296 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-532G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628296 | |||||||
| chr3:139628343 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-579G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628343 | |||||||
| chr3:139628448 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-684A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628448 | |||||||
| chr3:139628516 | A | G | 71 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(68): Show |
72 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-40-752T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628516 | |||||||
| chr3:139628626 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-862T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628626 | |||||||
| chr3:139628871 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-40-1107G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139628871 | |||||||
| chr3:139629023 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-40-1259C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629023 | |||||||
| chr3:139629280 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-40-1516C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629280 | |||||||
| chr3:139629310 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-1546C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629310 | |||||||
| chr3:139629331 | C | T | 14 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0178 others(11): Show |
14 | HG01123.hp1 HG01175.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-1567G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629331 | |||||||
| chr3:139629566 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-40-1802G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629566 | |||||||
| chr3:139629593 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-40-1829T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629593 | |||||||
| chr3:139629676 | T | C | 217 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
225 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-40-1912A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629676 | |||||||
| chr3:139629727 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-1963A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629727 | |||||||
| chr3:139629836 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG02630.hp2 HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-40-2072G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629836 | |||||||
| chr3:139629915 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-40-2151C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139629915 | |||||||
| chr3:139630417 | G | C | 14 | a0001c0001t0001g0162 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
16 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40-2653C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630417 | |||||||
| chr3:139630425 | G | T | 1 | a0001c0001t0001g0007 | 2 | NA18950.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-40-2661C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630425 | |||||||
| chr3:139630475 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-2711T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630475 | |||||||
| chr3:139630477 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-40-2713G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630477 | |||||||
| chr3:139630561 | C | A | 1 | a0001c0001t0004g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-2797G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630561 | |||||||
| chr3:139630580 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-40-2816G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630580 | |||||||
| chr3:139630581 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-40-2817C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630581 | |||||||
| chr3:139630701 | C | T | 10 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0026 others(7): Show |
10 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-2937G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630701 | |||||||
| chr3:139630766 | C | A | 1 | a0001c0001t0002g0012 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-40-3002G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139630766 | |||||||
| chr3:139631090 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-40-3326C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631090 | |||||||
| chr3:139631146 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-40-3382C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631146 | |||||||
| chr3:139631191 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-41+3420G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631191 | |||||||
| chr3:139631466 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+3145C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631466 | |||||||
| chr3:139631474 | T | C | 73 | a0001c0001t0001g0127 a0001c0001t0001g0132 a0001c0001t0001g0133 others(70): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-41+3137A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631474 | |||||||
| chr3:139631537 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-41+3074C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631537 | |||||||
| chr3:139631546 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-41+3065C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631546 | |||||||
| chr3:139631577 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-41+3034C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631577 | |||||||
| chr3:139631810 | C | T | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+2801G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631810 | |||||||
| chr3:139631811 | C | G | 218 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(215): Show |
226 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-41+2800G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631811 | |||||||
| chr3:139631818 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+2793G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631818 | |||||||
| chr3:139631852 | T | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+2759A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631852 | |||||||
| chr3:139631875 | T | G | 10 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+2736A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631875 | |||||||
| chr3:139631898 | T | A | 2 | a0001c0001t0003g0113 a0001c0001t0003g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-41+2713A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631898 | |||||||
| chr3:139631912 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-41+2699G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631912 | |||||||
| chr3:139631929 | T | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(51): Show |
55 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-41+2682A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139631929 | |||||||
| chr3:139632349 | A | G | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-41+2262T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632349 | |||||||
| chr3:139632357 | C | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0121 a0001c0001t0001g0125 others(104): Show |
110 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-41+2254G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632357 | |||||||
| chr3:139632464 | G | T | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-41+2147C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632464 | |||||||
| chr3:139632538 | G | A | 5 | a0001c0001t0001g0178 a0001c0003t0001g0192 a0001c0003t0002g0060 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+2073C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632538 | |||||||
| chr3:139632815 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0193 |
3 | HG02717.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-41+1796C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632815 | |||||||
| chr3:139632843 | T | C | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+1768A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632843 | |||||||
| chr3:139632856 | G | A | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+1755C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632856 | |||||||
| chr3:139632962 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-41+1649G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139632962 | |||||||
| chr3:139633040 | C | A | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+1571G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633040 | |||||||
| chr3:139633055 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-41+1556C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633055 | |||||||
| chr3:139633063 | G | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-41+1548C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633063 | |||||||
| chr3:139633064 | C | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-41+1547G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633064 | |||||||
| chr3:139633078 | G | A | 193 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
201 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-41+1533C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633078 | |||||||
| chr3:139633114 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-41+1497C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633114 | |||||||
| chr3:139633180 | G | GA | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(78): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-41+1430dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633180 | |||||||
| chr3:139633181 | A | AT | 21 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0131 others(18): Show |
21 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.-41+1429dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633181 | |||||||
| chr3:139633181 | AT | A | 22 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0125 others(19): Show |
23 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41+1429delA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633181 | |||||||
| chr3:139633182 | T | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0002g0069 |
3 | HG02155.hp2 HG03491.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-41+1429A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633182 | |||||||
| chr3:139633212 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-41+1399G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633212 | |||||||
| chr3:139633257 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-41+1354G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633257 | |||||||
| chr3:139633261 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(81): Show |
87 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+1350C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633261 | |||||||
| chr3:139633328 | G | A | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-41+1283C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633328 | |||||||
| chr3:139633369 | G | A | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-41+1242C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633369 | |||||||
| chr3:139633455 | C | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+1156G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633455 | |||||||
| chr3:139633566 | T | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(1): Show |
4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+1045A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633566 | |||||||
| chr3:139633724 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-41+887A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139633724 | |||||||
| chr3:139634349 | C | A | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+262G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139634349 | |||||||
| chr3:139634533 | C | T | 10 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
11 | HG01243.hp1 HG01496.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+78G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 3/6 | chr3 | 139634533 | |||||||
| chr3:139634764 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-77-117G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634764 | |||||||
| chr3:139634765 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-118C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634765 | |||||||
| chr3:139634822 | A | G | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
189 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-77-175T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634822 | |||||||
| chr3:139634867 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-77-220A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634867 | |||||||
| chr3:139634901 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-77-254A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139634901 | |||||||
| chr3:139635135 | A | G | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-77-488T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635135 | |||||||
| chr3:139635143 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-77-496A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635143 | |||||||
| chr3:139635192 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-77-545T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635192 | |||||||
| chr3:139635400 | G | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-77-753C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635400 | |||||||
| chr3:139635414 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-77-767C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635414 | |||||||
| chr3:139635438 | A | G | 3 | a0001c0002t0002g0001 a0001c0002t0002g0042 a0001c0002t0002g0043 |
4 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77-791T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635438 | |||||||
| chr3:139635531 | G | A | 2 | a0001c0001t0001g0185 a0004c0008t0001g0159 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-77-884C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635531 | |||||||
| chr3:139635564 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-917T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635564 | |||||||
| chr3:139635597 | GA | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG01243.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77-951delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635597 | |||||||
| chr3:139635729 | T | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0002g0052 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-77-1082A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139635729 | |||||||
| chr3:139636004 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-77-1357A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636004 | |||||||
| chr3:139636150 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-77-1503A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636150 | |||||||
| chr3:139636163 | G | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-77-1516C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636163 | |||||||
| chr3:139636205 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-77-1558A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636205 | |||||||
| chr3:139636303 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-77-1656G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636303 | |||||||
| chr3:139636335 | GA | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(65): Show |
73 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-78+1627delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636335 | |||||||
| chr3:139636420 | A | G | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-78+1543T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636420 | |||||||
| chr3:139636660 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-78+1303C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636660 | |||||||
| chr3:139636685 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-78+1278T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636685 | |||||||
| chr3:139636826 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-78+1137G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139636826 | |||||||
| chr3:139637360 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0002g0080 a0001c0001t0002g0081 |
3 | NA18957.hp2 NA18975.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-78+603A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637360 | |||||||
| chr3:139637446 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0040 |
2 | HG01496.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-78+517G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637446 | |||||||
| chr3:139637749 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-78+214G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637749 | |||||||
| chr3:139637923 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(56): Show |
63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-78+40C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637923 | |||||||
| chr3:139637954 | G | A | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(76): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.-78+9C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 2/6 | chr3 | 139637954 | |||||||
| chr3:139638216 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-177-154G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638216 | |||||||
| chr3:139638251 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.-177-189C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638251 | |||||||
| chr3:139638269 | G | T | 3 | a0001c0001t0001g0201 a0001c0001t0002g0024 a0001c0001t0002g0025 |
3 | NA18964.hp1 NA19005.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-177-207C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638269 | |||||||
| chr3:139638396 | A | C | 2 | a0001c0001t0002g0023 a0001c0001t0005g0010 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177-334T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638396 | |||||||
| chr3:139638402 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-340C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638402 | |||||||
| chr3:139638410 | T | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0230 a0001c0001t0001g0253 others(8): Show |
12 | HG01192.hp1 HG02165.hp2 HG02273.hp1 others(9): Show |
intron_variant | MODIFIER | c.-177-348A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638410 | |||||||
| chr3:139638457 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-395C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638457 | |||||||
| chr3:139638495 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-177-433C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638495 | |||||||
| chr3:139638537 | GC | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-476delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638537 | |||||||
| chr3:139638576 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-177-514C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638576 | |||||||
| chr3:139638685 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-623A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638685 | |||||||
| chr3:139638999 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-937T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139638999 | |||||||
| chr3:139639081 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(1): Show |
4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-1019G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639081 | |||||||
| chr3:139639162 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-177-1100G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639162 | |||||||
| chr3:139639311 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1249C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639311 | |||||||
| chr3:139639366 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0210 |
2 | HG00280.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-177-1304C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639366 | |||||||
| chr3:139639382 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-1320C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639382 | |||||||
| chr3:139639396 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1334T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639396 | |||||||
| chr3:139639415 | A | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1353T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639415 | |||||||
| chr3:139639484 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1422C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639484 | |||||||
| chr3:139639504 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-1442C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639504 | |||||||
| chr3:139639715 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1653G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639715 | |||||||
| chr3:139639912 | C | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-1850G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139639912 | |||||||
| chr3:139640140 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-2078C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640140 | |||||||
| chr3:139640140 | G | T | 1 | a0001c0001t0002g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-177-2078C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640140 | |||||||
| chr3:139640193 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-177-2131C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640193 | |||||||
| chr3:139640568 | T | C | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-177-2506A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640568 | |||||||
| chr3:139640667 | C | T | 2 | a0001c0001t0001g0185 a0004c0008t0001g0159 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-177-2605G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640667 | |||||||
| chr3:139640691 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(60): Show |
67 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-177-2629T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640691 | |||||||
| chr3:139640737 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-177-2675G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640737 | |||||||
| chr3:139640872 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-2810C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640872 | |||||||
| chr3:139640965 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2903T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640965 | |||||||
| chr3:139640970 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2908A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640970 | |||||||
| chr3:139640971 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2909T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640971 | |||||||
| chr3:139640972 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2910T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640972 | |||||||
| chr3:139640974 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2912G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640974 | |||||||
| chr3:139640978 | A | AATTATAT others(15): Show |
1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2917_-177-291 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640978 | |||||||
| chr3:139640996 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2934A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640996 | |||||||
| chr3:139640997 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2935T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139640997 | |||||||
| chr3:139641000 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2938G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641000 | |||||||
| chr3:139641003 | GAACGGTA others(18): Show |
G | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2966_-177-294 others(29): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641003 | |||||||
| chr3:139641029 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2967T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641029 | |||||||
| chr3:139641037 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-177-2975G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641037 | |||||||
| chr3:139641081 | C | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3019G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641081 | |||||||
| chr3:139641183 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-177-3121T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641183 | |||||||
| chr3:139641223 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-177-3161A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641223 | |||||||
| chr3:139641383 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3321C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641383 | |||||||
| chr3:139641401 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3339G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641401 | |||||||
| chr3:139641599 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3537C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641599 | |||||||
| chr3:139641614 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-3552T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641614 | |||||||
| chr3:139641657 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-177-3595G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641657 | |||||||
| chr3:139641665 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-177-3603A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641665 | |||||||
| chr3:139641743 | A | G | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-3681T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139641743 | |||||||
| chr3:139642085 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-177-4023G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642085 | |||||||
| chr3:139642101 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-177-4039C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642101 | |||||||
| chr3:139642187 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-177-4125A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642187 | |||||||
| chr3:139642210 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-4148T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642210 | |||||||
| chr3:139642227 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-177-4165T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642227 | |||||||
| chr3:139642397 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-4335C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642397 | |||||||
| chr3:139642522 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01243.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-4460C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642522 | |||||||
| chr3:139642598 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-177-4536G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642598 | |||||||
| chr3:139642900 | C | G | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177-4838G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642900 | |||||||
| chr3:139642991 | G | T | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-177-4929C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139642991 | |||||||
| chr3:139643126 | A | T | 9 | a0001c0001t0001g0266 a0001c0001t0001g0278 a0001c0001t0001g0309 others(6): Show |
9 | HG02523.hp2 NA18612.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-5064T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643126 | |||||||
| chr3:139643297 | A | T | 1 | a0001c0001t0001g0254 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-177-5235T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643297 | |||||||
| chr3:139643383 | A | C | 1 | a0001c0001t0001g0305 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-177-5321T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643383 | |||||||
| chr3:139643391 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-5329A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643391 | |||||||
| chr3:139643471 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0002g0023 |
2 | HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-5409A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643471 | |||||||
| chr3:139643517 | C | T | 2 | a0001c0001t0001g0178 a0001c0003t0001g0192 |
2 | HG01433.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-177-5455G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643517 | |||||||
| chr3:139643714 | C | T | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-5652G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643714 | |||||||
| chr3:139643719 | G | A | 40 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(37): Show |
41 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.-177-5657C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139643719 | |||||||
| chr3:139644026 | C | A | 4 | a0001c0001t0002g0052 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-5964G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644026 | |||||||
| chr3:139644222 | A | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0002g0052 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-6160T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644222 | |||||||
| chr3:139644226 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-177-6164G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644226 | |||||||
| chr3:139644270 | A | G | 4 | a0001c0001t0002g0052 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-6208T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644270 | |||||||
| chr3:139644348 | T | C | 14 | a0001c0001t0001g0162 a0001c0001t0001g0187 a0001c0001t0001g0188 others(11): Show |
16 | HG01884.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-6286A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644348 | |||||||
| chr3:139644465 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-6403G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644465 | |||||||
| chr3:139644601 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177-6539C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644601 | |||||||
| chr3:139644721 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177-6659T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644721 | |||||||
| chr3:139644925 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0002g0088 a0001c0003t0001g0192 others(3): Show |
6 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177-6863G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139644925 | |||||||
| chr3:139645074 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-177-7012G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645074 | |||||||
| chr3:139645169 | T | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-7107A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645169 | |||||||
| chr3:139645337 | A | G | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-7275T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645337 | |||||||
| chr3:139645374 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-177-7312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645374 | |||||||
| chr3:139645464 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(56): Show |
63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-177-7402C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645464 | |||||||
| chr3:139645552 | C | T | 11 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(8): Show |
11 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-177-7490G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645552 | |||||||
| chr3:139645564 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-7502C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645564 | |||||||
| chr3:139645764 | T | C | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-7702A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645764 | |||||||
| chr3:139645833 | T | A | 1 | a0001c0001t0001g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-177-7771A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645833 | |||||||
| chr3:139645861 | C | T | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-177-7799G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645861 | |||||||
| chr3:139645862 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-177-7800C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645862 | |||||||
| chr3:139645870 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-177-7808A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645870 | |||||||
| chr3:139645943 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-7881C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139645943 | |||||||
| chr3:139646089 | GGGT | G | 9 | a0001c0001t0001g0160 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG01255.hp1 HG02523.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-8030_-177-802 others(7): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646089 | |||||||
| chr3:139646190 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-8128C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646190 | |||||||
| chr3:139646222 | A | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0002g0023 |
3 | HG02145.hp1 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-177-8160T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646222 | |||||||
| chr3:139646389 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-8327T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646389 | |||||||
| chr3:139646394 | T | C | 1 | a0001c0003t0002g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-177-8332A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646394 | |||||||
| chr3:139646439 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-177-8377A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646439 | |||||||
| chr3:139646485 | C | T | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-8423G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646485 | |||||||
| chr3:139646725 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(55): Show |
61 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-177-8663C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646725 | |||||||
| chr3:139646837 | A | C | 1 | a0001c0001t0002g0076 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-177-8775T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646837 | |||||||
| chr3:139646969 | A | G | 3 | a0001c0001t0001g0293 a0001c0001t0002g0022 a0001c0001t0002g0075 |
3 | HG02027.hp2 NA18962.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-177-8907T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139646969 | |||||||
| chr3:139647166 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-177-9104T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647166 | |||||||
| chr3:139647291 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-177-9229A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647291 | |||||||
| chr3:139647300 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-9238G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647300 | |||||||
| chr3:139647306 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(57): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-9244T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647306 | |||||||
| chr3:139647487 | T | C | 18 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0013 others(15): Show |
18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177-9425A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647487 | |||||||
| chr3:139647846 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-177-9784A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647846 | |||||||
| chr3:139647849 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-177-9787G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139647849 | |||||||
| chr3:139648065 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-10003A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648065 | |||||||
| chr3:139648109 | G | A | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-10047C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648109 | |||||||
| chr3:139648201 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0124 others(58): Show |
64 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.-177-10139A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648201 | |||||||
| chr3:139648283 | T | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(102): Show |
108 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-177-10221A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648283 | |||||||
| chr3:139648430 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-177-10368A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648430 | |||||||
| chr3:139648821 | G | A | 1 | a0001c0001t0011g0154 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-177-10759C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648821 | |||||||
| chr3:139648917 | TTATAA | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(55): Show |
61 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-177-10860_-177-10 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139648917 | |||||||
| chr3:139649002 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-177-10940T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649002 | |||||||
| chr3:139649002 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-10940T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649002 | |||||||
| chr3:139649204 | C | T | 6 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0002g0052 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-11142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649204 | |||||||
| chr3:139649211 | C | A | 7 | a0001c0001t0001g0178 a0001c0001t0002g0088 a0001c0001t0005g0009 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-11149G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649211 | |||||||
| chr3:139649271 | T | C | 62 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0124 others(59): Show |
65 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-177-11209A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649271 | |||||||
| chr3:139649322 | A | AAAAC | 40 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0125 others(37): Show |
40 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-177-11264_-177-11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | |||||||
| chr3:139649322 | A | AAAACAAA others(1): Show |
134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-177-11268_-177-11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | |||||||
| chr3:139649322 | A | AAAACAAA others(5): Show |
2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-177-11272_-177-11 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649322 | |||||||
| chr3:139649432 | C | T | 1 | a0001c0001t0005g0010 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-177-11370G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649432 | |||||||
| chr3:139649520 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-177-11458T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649520 | |||||||
| chr3:139649762 | C | G | 1 | a0001c0001t0002g0040 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-177-11700G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649762 | |||||||
| chr3:139649764 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
5 | HG01192.hp2 HG01257.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-11702G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649764 | |||||||
| chr3:139649968 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-11906G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139649968 | |||||||
| chr3:139650079 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(59): Show |
66 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.-177-12017A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650079 | |||||||
| chr3:139650440 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-177-12378T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650440 | |||||||
| chr3:139650717 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-12655G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650717 | |||||||
| chr3:139650925 | T | A | 18 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0013 others(15): Show |
18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-177-12863A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139650925 | |||||||
| chr3:139651262 | T | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(1): Show |
4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-13200A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651262 | |||||||
| chr3:139651412 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(77): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-177-13350T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651412 | |||||||
| chr3:139651740 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-177-13678C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651740 | |||||||
| chr3:139651812 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-177-13750G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651812 | |||||||
| chr3:139651937 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0109 |
2 | HG01255.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-177-13875C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139651937 | |||||||
| chr3:139652122 | G | A | 7 | a0001c0001t0001g0178 a0001c0001t0002g0088 a0001c0001t0005g0009 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-14060C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652122 | |||||||
| chr3:139652167 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-177-14105A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652167 | |||||||
| chr3:139652224 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-14162G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652224 | |||||||
| chr3:139652323 | A | C | 21 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0163 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-177-14261T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652323 | |||||||
| chr3:139652355 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-177-14293A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652355 | |||||||
| chr3:139652753 | C | T | 8 | a0001c0001t0001g0178 a0001c0001t0001g0193 a0001c0001t0002g0088 others(5): Show |
8 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-177-14691G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652753 | |||||||
| chr3:139652923 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-14861C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652923 | |||||||
| chr3:139652924 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0002g0012 a0001c0001t0002g0040 others(2): Show |
5 | HG01099.hp2 HG01496.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-14862G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139652924 | |||||||
| chr3:139653109 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-15047C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653109 | |||||||
| chr3:139653209 | A | T | 10 | a0001c0001t0001g0127 a0001c0001t0001g0173 a0001c0001t0001g0204 others(7): Show |
10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-15147T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653209 | |||||||
| chr3:139653313 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0303 |
2 | NA18961.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-177-15251C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653313 | |||||||
| chr3:139653454 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-15392G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653454 | |||||||
| chr3:139653491 | A | G | 2 | a0001c0001t0002g0023 a0001c0001t0005g0010 |
2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177-15429T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653491 | |||||||
| chr3:139653576 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-177-15514C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653576 | |||||||
| chr3:139653580 | C | A | 12 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0181 others(9): Show |
13 | HG01099.hp2 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.-177-15518G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653580 | |||||||
| chr3:139653681 | G | A | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-15619C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653681 | |||||||
| chr3:139653824 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0287 others(1): Show |
5 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177-15762C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653824 | |||||||
| chr3:139653834 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-177-15772C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653834 | |||||||
| chr3:139653914 | A | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0121 others(83): Show |
91 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-177-15852T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653914 | |||||||
| chr3:139653954 | C | G | 1 | a0001c0001t0002g0035 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-177-15892G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139653954 | |||||||
| chr3:139654145 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-177-16083C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654145 | |||||||
| chr3:139654346 | G | A | 10 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-16284C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654346 | |||||||
| chr3:139654385 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-177-16323C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654385 | |||||||
| chr3:139654657 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0270 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-177-16595A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654657 | |||||||
| chr3:139654718 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-177-16656A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654718 | |||||||
| chr3:139654725 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0283 a0001c0001t0002g0068 |
3 | HG00621.hp1 NA18747.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-177-16663T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654725 | |||||||
| chr3:139654851 | C | T | 6 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0002g0052 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-16789G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654851 | |||||||
| chr3:139654870 | GAC | G | 10 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-16810_-177-16 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654870 | |||||||
| chr3:139654935 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-16873G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139654935 | |||||||
| chr3:139655004 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0109 others(1): Show |
4 | HG01109.hp1 HG01255.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177-16942C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655004 | |||||||
| chr3:139655123 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-17061G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655123 | |||||||
| chr3:139655194 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-177-17132C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655194 | |||||||
| chr3:139655209 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-177-17147C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655209 | |||||||
| chr3:139655209 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-17147C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655209 | |||||||
| chr3:139655261 | T | G | 15 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-177-17199A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655261 | |||||||
| chr3:139655285 | T | C | 4 | a0001c0001t0002g0052 a0001c0002t0002g0001 a0001c0002t0002g0042 others(1): Show |
5 | HG01496.hp2 HG02257.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-17223A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655285 | |||||||
| chr3:139655299 | C | T | 12 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0178 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177-17237G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655299 | |||||||
| chr3:139655313 | G | A | 12 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0178 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177-17251C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655313 | |||||||
| chr3:139655626 | T | TGAA | 199 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
207 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.-177-17567_-177-17 others(9): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655626 | |||||||
| chr3:139655696 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18977.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-177-17634G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139655696 | |||||||
| chr3:139656113 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-177-18051A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656113 | |||||||
| chr3:139656177 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-177-18115C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656177 | |||||||
| chr3:139656345 | TCTA | T | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18286_-177-18 others(9): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656345 | |||||||
| chr3:139656349 | A | G | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18287T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656349 | |||||||
| chr3:139656351 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(7): Show |
10 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-18289C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656351 | |||||||
| chr3:139656396 | C | T | 10 | a0001c0001t0001g0178 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-18334G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656396 | |||||||
| chr3:139656450 | G | A | 10 | a0001c0001t0001g0127 a0001c0001t0001g0173 a0001c0001t0001g0204 others(7): Show |
10 | HG00733.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177-18388C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656450 | |||||||
| chr3:139656549 | AG | A | 19 | a0001c0001t0001g0185 a0001c0001t0001g0209 a0001c0001t0001g0266 others(16): Show |
19 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-177-18488delC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656549 | |||||||
| chr3:139656607 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(92): Show |
98 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-177-18545C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656607 | |||||||
| chr3:139656610 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-177-18548T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656610 | |||||||
| chr3:139656650 | G | T | 6 | a0001c0001t0001g0121 a0001c0001t0001g0181 a0001c0001t0002g0052 others(3): Show |
7 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177-18588C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656650 | |||||||
| chr3:139656783 | C | A | 19 | a0001c0001t0001g0185 a0001c0001t0001g0209 a0001c0001t0001g0266 others(16): Show |
19 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-177-18721G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656783 | |||||||
| chr3:139656844 | AATCTT | A | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 |
3 | HG01192.hp2 HG01257.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-177-18787_-177-18 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656844 | |||||||
| chr3:139656846 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-177-18784A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656846 | |||||||
| chr3:139656872 | T | G | 1 | a0001c0001t0002g0067 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-177-18810A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656872 | |||||||
| chr3:139656909 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-177-18847G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656909 | |||||||
| chr3:139656912 | G | A | 196 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-177-18850C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656912 | |||||||
| chr3:139656974 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-177-18912G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139656974 | |||||||
| chr3:139657015 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-177-18953A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657015 | |||||||
| chr3:139657582 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-177-19520C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657582 | |||||||
| chr3:139657670 | G | A | 15 | a0001c0001t0001g0209 a0001c0001t0001g0266 a0001c0001t0001g0278 others(12): Show |
15 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-19608C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657670 | |||||||
| chr3:139657688 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-177-19626C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657688 | |||||||
| chr3:139657858 | AGT | A | 15 | a0001c0001t0001g0209 a0001c0001t0001g0266 a0001c0001t0001g0278 others(12): Show |
15 | HG01192.hp2 HG01257.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-19798_-177-19 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657858 | |||||||
| chr3:139657906 | G | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0129 others(58): Show |
65 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.-178+19799C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657906 | |||||||
| chr3:139657913 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-178+19792C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657913 | |||||||
| chr3:139657967 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-178+19738A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139657967 | |||||||
| chr3:139658184 | G | A | 60 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(57): Show |
63 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.-178+19521C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658184 | |||||||
| chr3:139658355 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0002g0052 a0001c0002t0002g0001 others(2): Show |
6 | HG01496.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-178+19350G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658355 | |||||||
| chr3:139658425 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0003g0177 |
3 | HG00735.hp2 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-178+19280A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658425 | |||||||
| chr3:139658433 | C | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(74): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-178+19272G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658433 | |||||||
| chr3:139658479 | T | A | 211 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(208): Show |
218 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-178+19226A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658479 | |||||||
| chr3:139658502 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-178+19203G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658502 | |||||||
| chr3:139658564 | T | C | 210 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-178+19141A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658564 | |||||||
| chr3:139658661 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-178+19044G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658661 | |||||||
| chr3:139658668 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-178+19037A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658668 | |||||||
| chr3:139658778 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0287 a0001c0001t0001g0288 others(2): Show |
5 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-178+18927C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658778 | |||||||
| chr3:139658886 | TC | T | 206 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
213 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-178+18818delG | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658886 | |||||||
| chr3:139658949 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-178+18756C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139658949 | |||||||
| chr3:139659002 | C | T | 2 | a0001c0001t0002g0012 a0004c0008t0001g0159 |
2 | HG01099.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-178+18703G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659002 | |||||||
| chr3:139659219 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-178+18486A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659219 | |||||||
| chr3:139659313 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0099 others(90): Show |
96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-178+18392T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659313 | |||||||
| chr3:139659543 | T | C | 19 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0011 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+18162A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659543 | |||||||
| chr3:139659597 | TA | T | 17 | a0001c0001t0001g0209 a0001c0001t0001g0266 a0001c0001t0001g0278 others(14): Show |
17 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+18107delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659597 | |||||||
| chr3:139659730 | C | A | 11 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0190 others(8): Show |
11 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+17975G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659730 | |||||||
| chr3:139659760 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-178+17945T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659760 | |||||||
| chr3:139659789 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-178+17916G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139659789 | |||||||
| chr3:139660142 | G | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0099 others(90): Show |
96 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.-178+17563C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660142 | |||||||
| chr3:139660169 | A | C | 19 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0011 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17536T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660169 | |||||||
| chr3:139660321 | A | G | 19 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0011 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17384T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660321 | |||||||
| chr3:139660358 | T | C | 79 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0126 others(76): Show |
83 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.-178+17347A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660358 | |||||||
| chr3:139660463 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-178+17242A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660463 | |||||||
| chr3:139660476 | A | G | 19 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0011 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-178+17229T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660476 | |||||||
| chr3:139660543 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0130 others(77): Show |
83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-178+17162C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660543 | |||||||
| chr3:139660832 | TA | T | 210 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-178+16872delT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660832 | |||||||
| chr3:139660913 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-178+16792T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139660913 | |||||||
| chr3:139661006 | T | G | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0004c0008t0001g0159 |
3 | HG01099.hp2 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-178+16699A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661006 | |||||||
| chr3:139661098 | C | T | 18 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0013 others(15): Show |
18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-178+16607G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661098 | |||||||
| chr3:139661215 | A | C | 18 | a0001c0001t0001g0209 a0001c0001t0001g0266 a0001c0001t0001g0278 others(15): Show |
18 | HG01099.hp2 HG01192.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-178+16490T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661215 | |||||||
| chr3:139661255 | T | A | 1 | a0001c0001t0002g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-178+16450A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661255 | |||||||
| chr3:139661293 | G | A | 10 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0190 others(7): Show |
10 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-178+16412C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661293 | |||||||
| chr3:139661305 | C | G | 18 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0013 others(15): Show |
18 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-178+16400G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661305 | |||||||
| chr3:139661352 | G | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0179 others(4): Show |
7 | HG01175.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+16353C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661352 | |||||||
| chr3:139661388 | G | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0181 others(4): Show |
8 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-178+16317C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661388 | |||||||
| chr3:139661475 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-178+16230A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661475 | |||||||
| chr3:139661631 | C | T | 57 | a0001c0001t0001g0008 a0001c0001t0001g0129 a0001c0001t0001g0161 others(54): Show |
60 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-178+16074G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661631 | |||||||
| chr3:139661924 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0287 others(3): Show |
7 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+15781C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139661924 | |||||||
| chr3:139662374 | G | T | 1 | a0001c0001t0001g0297 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-178+15331C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662374 | |||||||
| chr3:139662726 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0031 a0001c0001t0002g0032 |
3 | HG00639.hp1 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-178+14979C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662726 | |||||||
| chr3:139662983 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0181 a0001c0001t0002g0013 others(4): Show |
8 | HG01496.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+14722C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139662983 | |||||||
| chr3:139663005 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-178+14700T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663005 | |||||||
| chr3:139663237 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-178+14468A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663237 | |||||||
| chr3:139663380 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | NA18946.hp1 NA18972.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-178+14325G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663380 | |||||||
| chr3:139663570 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-178+14135A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663570 | |||||||
| chr3:139663773 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0193 |
2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-178+13932G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663773 | |||||||
| chr3:139663937 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-178+13768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663937 | |||||||
| chr3:139663966 | G | GT | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0220 others(1): Show |
4 | HG02145.hp2 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+13738dupA | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139663966 | |||||||
| chr3:139664349 | T | A | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+13356A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664349 | |||||||
| chr3:139664416 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0006g0044 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-178+13289G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664416 | |||||||
| chr3:139664976 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG02145.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-178+12729A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139664976 | |||||||
| chr3:139665098 | A | G | 1 | a0001c0004t0001g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-178+12607T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665098 | |||||||
| chr3:139665156 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-178+12549C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665156 | |||||||
| chr3:139665252 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+12453G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665252 | |||||||
| chr3:139665406 | G | C | 5 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(2): Show |
5 | HG00735.hp1 HG01515.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+12299C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665406 | |||||||
| chr3:139665539 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-178+12166A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665539 | |||||||
| chr3:139665725 | G | GGA | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
141 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-178+11978_-178+11 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | G | GGAGA | 12 | a0001c0001t0001g0128 a0001c0001t0001g0146 a0001c0001t0001g0176 others(9): Show |
12 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11976_-178+11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | G | GGAGAGA | 8 | a0001c0001t0001g0121 a0001c0001t0001g0178 a0001c0001t0001g0179 others(5): Show |
8 | HG01175.hp1 HG02145.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+11974_-178+11 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | G | GGAGAGAG others(1): Show |
6 | a0001c0001t0001g0180 a0001c0002t0001g0122 a0001c0002t0001g0123 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-178+11972_-178+11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | G | GGAGAGAG others(3): Show |
4 | a0001c0001t0001g0124 a0001c0001t0001g0181 a0001c0001t0001g0263 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+11970_-178+11 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | GGA | G | 73 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(70): Show |
75 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.-178+11978_-178+11 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | GGAGA | G | 3 | a0001c0001t0001g0185 a0001c0001t0002g0014 a0001c0001t0002g0015 |
3 | HG02486.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-178+11976_-178+11 others(10): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | GGAGAGA | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0183 a0001c0001t0002g0093 |
3 | HG03688.hp1 HG04204.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-178+11974_-178+11 others(12): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665725 | GGAGAGAG others(1): Show |
G | 50 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(47): Show |
50 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-178+11972_-178+11 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665725 | |||||||
| chr3:139665836 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0270 |
2 | HG02602.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-178+11869T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139665836 | |||||||
| chr3:139666132 | C | T | 11 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0272 others(8): Show |
11 | HG02071.hp1 HG02165.hp2 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.-178+11573G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666132 | |||||||
| chr3:139666133 | G | A | 12 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0189 others(9): Show |
12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11572C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666133 | |||||||
| chr3:139666186 | C | A | 12 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0189 others(9): Show |
12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+11519G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666186 | |||||||
| chr3:139666215 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-178+11490G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666215 | |||||||
| chr3:139666336 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-178+11369G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666336 | |||||||
| chr3:139666415 | G | A | 228 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(225): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-178+11290C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666415 | |||||||
| chr3:139666444 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-178+11261T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666444 | |||||||
| chr3:139666554 | C | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0195 others(61): Show |
66 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-178+11151G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666554 | |||||||
| chr3:139666591 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0128 a0001c0001t0001g0131 others(19): Show |
23 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-178+11114G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666591 | |||||||
| chr3:139666892 | C | G | 12 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0189 others(9): Show |
12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+10813G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666892 | |||||||
| chr3:139666896 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-178+10809C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666896 | |||||||
| chr3:139666901 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-178+10804A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666901 | |||||||
| chr3:139666912 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-178+10793C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139666912 | |||||||
| chr3:139667015 | G | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+10690C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667015 | |||||||
| chr3:139667039 | T | C | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+10666A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667039 | |||||||
| chr3:139667081 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+10624T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667081 | |||||||
| chr3:139667671 | T | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0125 others(57): Show |
62 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-178+10034A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667671 | |||||||
| chr3:139667712 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-178+9993T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667712 | |||||||
| chr3:139667746 | T | A | 9 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0189 others(6): Show |
9 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-178+9959A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667746 | |||||||
| chr3:139667873 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-178+9832A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139667873 | |||||||
| chr3:139668108 | C | G | 1 | a0001c0004t0001g0119 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-178+9597G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668108 | |||||||
| chr3:139668357 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+9348T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668357 | |||||||
| chr3:139668441 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-178+9264T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668441 | |||||||
| chr3:139668850 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00280.hp1 HG00639.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-178+8855T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139668850 | |||||||
| chr3:139669015 | G | A | 24 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0002g0002 others(21): Show |
28 | HG00099.hp2 HG00738.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-178+8690C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669015 | |||||||
| chr3:139669029 | T | A | 12 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0001g0189 others(9): Show |
12 | HG01175.hp1 HG01243.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-178+8676A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669029 | |||||||
| chr3:139669198 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0002g0061 |
2 | HG01243.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-178+8507G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669198 | |||||||
| chr3:139669264 | G | C | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-178+8441C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669264 | |||||||
| chr3:139669455 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-178+8250G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669455 | |||||||
| chr3:139669476 | C | CA | 10 | a0001c0001t0001g0202 a0001c0001t0001g0237 a0001c0001t0001g0239 others(7): Show |
10 | HG01255.hp1 NA18966.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-178+8228dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669476 | |||||||
| chr3:139669477 | AG | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0195 others(41): Show |
46 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.-178+8227delC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669477 | |||||||
| chr3:139669478 | G | A | 17 | a0001c0001t0001g0202 a0001c0001t0001g0233 a0001c0001t0001g0234 others(14): Show |
17 | HG01123.hp2 HG01255.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-178+8227C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | |||||||
| chr3:139669478 | G | GA | 66 | a0001c0001t0001g0106 a0001c0001t0001g0126 a0001c0001t0001g0130 others(63): Show |
68 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-178+8226dupT | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | |||||||
| chr3:139669478 | G | GAA | 11 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG01167.hp2 HG01891.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+8225_-178+822 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | |||||||
| chr3:139669478 | GAAAAAAA | G | 17 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0272 others(14): Show |
17 | HG01192.hp2 HG01256.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+8220_-178+822 others(11): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669478 | |||||||
| chr3:139669971 | C | T | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+7734G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139669971 | |||||||
| chr3:139670103 | G | T | 24 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0002g0002 others(21): Show |
28 | HG00099.hp2 HG00738.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-178+7602C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670103 | |||||||
| chr3:139670222 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-178+7483G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670222 | |||||||
| chr3:139670242 | G | A | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | HG01099.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+7463C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670242 | |||||||
| chr3:139670408 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-178+7297A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670408 | |||||||
| chr3:139670420 | C | T | 4 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(1): Show |
4 | HG00639.hp1 HG01074.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+7285G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670420 | |||||||
| chr3:139670504 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-178+7201T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670504 | |||||||
| chr3:139670511 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0183 |
2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-178+7194T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670511 | |||||||
| chr3:139670758 | T | C | 9 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0029 others(6): Show |
9 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-178+6947A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670758 | |||||||
| chr3:139670782 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-178+6923A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670782 | |||||||
| chr3:139670910 | A | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0053 |
2 | HG00738.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-178+6795T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139670910 | |||||||
| chr3:139671078 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+6627T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671078 | |||||||
| chr3:139671234 | C | T | 5 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0034 others(2): Show |
5 | HG01069.hp2 HG01106.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+6471G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671234 | |||||||
| chr3:139671478 | T | C | 1 | a0001c0003t0002g0090 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-178+6227A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671478 | |||||||
| chr3:139671552 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-178+6153G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671552 | |||||||
| chr3:139671618 | T | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0002c0005t0002g0033 |
3 | HG02965.hp1 NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-178+6087A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | |||||||
| chr3:139671618 | T | TCA | 63 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0125 others(60): Show |
65 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-178+6085_-178+608 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | |||||||
| chr3:139671618 | T | TCACA | 65 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0195 others(62): Show |
67 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-178+6083_-178+608 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671618 | |||||||
| chr3:139671620 | A | T | 4 | a0001c0001t0001g0128 a0001c0001t0002g0013 a0001c0004t0001g0119 others(1): Show |
4 | HG01175.hp2 HG02055.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+6085T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671620 | |||||||
| chr3:139671657 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+6048G>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671657 | |||||||
| chr3:139671971 | G | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-178+5734C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671971 | |||||||
| chr3:139671977 | G | A | 5 | a0001c0001t0002g0088 a0001c0003t0001g0192 a0001c0003t0002g0060 others(2): Show |
5 | HG01123.hp1 HG01433.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+5728C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671977 | |||||||
| chr3:139671997 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-178+5708A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671997 | |||||||
| chr3:139671997 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-178+5708A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139671997 | |||||||
| chr3:139672031 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-178+5674G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672031 | |||||||
| chr3:139672111 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0050 a0001c0001t0002g0051 |
4 | HG00099.hp2 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+5594A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672111 | |||||||
| chr3:139672114 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-178+5591C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672114 | |||||||
| chr3:139672156 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-178+5549G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672156 | |||||||
| chr3:139672219 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-178+5486T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672219 | |||||||
| chr3:139672290 | G | T | 49 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(46): Show |
49 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-178+5415C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672290 | |||||||
| chr3:139672326 | T | C | 91 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0203 others(88): Show |
95 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.-178+5379A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672326 | |||||||
| chr3:139672332 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-178+5373G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672332 | |||||||
| chr3:139672388 | T | C | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-178+5317A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672388 | |||||||
| chr3:139672619 | T | TG | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0003t0002g0060 others(2): Show |
5 | HG01123.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+5085dupC | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672619 | |||||||
| chr3:139672643 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-178+5062T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139672643 | |||||||
| chr3:139673105 | C | T | 1 | a0004c0008t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-178+4600G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673105 | |||||||
| chr3:139673162 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-178+4543C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673162 | |||||||
| chr3:139673239 | T | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0023 |
3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+4466A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673239 | |||||||
| chr3:139673264 | G | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0023 |
3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+4441C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673264 | |||||||
| chr3:139673304 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-178+4401G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673304 | |||||||
| chr3:139673356 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-178+4349A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673356 | |||||||
| chr3:139673367 | T | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0309 others(1): Show |
4 | NA18941.hp1 NA18969.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+4338A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673367 | |||||||
| chr3:139673473 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0091 |
3 | NA18942.hp2 NA18964.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-178+4232C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673473 | |||||||
| chr3:139673526 | T | C | 231 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-178+4179A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673526 | |||||||
| chr3:139673563 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02015.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.-178+4142G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673563 | |||||||
| chr3:139673585 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-178+4120G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673585 | |||||||
| chr3:139673693 | A | G | 85 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0002g0002 others(82): Show |
89 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-178+4012T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673693 | |||||||
| chr3:139673816 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-178+3889C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673816 | |||||||
| chr3:139673904 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG01167.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+3801G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673904 | |||||||
| chr3:139673998 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0023 |
3 | HG01099.hp2 HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+3707G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673998 | |||||||
| chr3:139673999 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-178+3706C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139673999 | |||||||
| chr3:139674078 | G | T | 1 | a0001c0003t0002g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-178+3627C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674078 | |||||||
| chr3:139674079 | A | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
84 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.-178+3626T>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674079 | |||||||
| chr3:139674080 | T | C | 216 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(213): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-178+3625A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674080 | |||||||
| chr3:139674109 | C | T | 207 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.-178+3596G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674109 | |||||||
| chr3:139674278 | G | A | 1 | a0002c0005t0002g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-178+3427C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674278 | |||||||
| chr3:139674289 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-178+3416C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674289 | |||||||
| chr3:139674379 | C | T | 11 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(8): Show |
11 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+3326G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674379 | |||||||
| chr3:139674523 | G | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
83 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-178+3182C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674523 | |||||||
| chr3:139674626 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-178+3079G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674626 | |||||||
| chr3:139674640 | T | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+3065A>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674640 | |||||||
| chr3:139674769 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 |
3 | HG01069.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-178+2936C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674769 | |||||||
| chr3:139674800 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-178+2905A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674800 | |||||||
| chr3:139674871 | T | C | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+2834A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674871 | |||||||
| chr3:139674991 | T | C | 83 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
87 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-178+2714A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674991 | |||||||
| chr3:139674998 | G | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+2707C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139674998 | |||||||
| chr3:139675135 | T | TAC | 47 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(44): Show |
47 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-178+2568_-178+256 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(3): Show |
74 | a0001c0001t0001g0006 a0001c0001t0001g0195 a0001c0001t0001g0197 others(71): Show |
75 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-178+2560_-178+256 others(14): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(5): Show |
45 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0185 others(42): Show |
47 | HG00621.hp1 HG00621.hp2 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.-178+2558_-178+256 others(16): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00423.hp1 HG02896.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+2556_-178+256 others(18): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(9): Show |
11 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(8): Show |
11 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(15): Show |
2 | a0001c0001t0002g0092 a0001c0001t0002g0093 |
2 | HG01169.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(26): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(17): Show |
41 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0024 others(38): Show |
41 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(28): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(19): Show |
24 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(21): Show |
28 | HG00099.hp2 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-178+2569_-178+257 others(30): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(9): Show |
2 | a0001c0001t0002g0011 a0001c0001t0002g0023 |
2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+2554_-178+256 others(20): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | T | TACACACA others(11): Show |
2 | a0001c0001t0001g0313 a0001c0001t0002g0012 |
2 | HG01099.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-178+2552_-178+256 others(22): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675135 | TAC | T | 15 | a0001c0001t0001g0121 a0001c0001t0001g0124 a0001c0001t0002g0013 others(12): Show |
15 | HG01081.hp1 HG01175.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+2568_-178+256 others(6): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675135 | |||||||
| chr3:139675197 | G | T | 11 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(8): Show |
11 | HG00639.hp1 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-178+2508C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675197 | |||||||
| chr3:139675311 | G | A | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+2394C>T | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675311 | |||||||
| chr3:139675362 | A | G | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+2343T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675362 | |||||||
| chr3:139675393 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-178+2312T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675393 | |||||||
| chr3:139675399 | CAGTT | C | 46 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0024 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-178+2302_-178+230 others(8): Show |
NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675399 | |||||||
| chr3:139675679 | C | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0002g0024 others(1): Show |
4 | HG02145.hp2 HG02602.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+2026G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675679 | |||||||
| chr3:139675729 | T | C | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+1976A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675729 | |||||||
| chr3:139675743 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-178+1962C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675743 | |||||||
| chr3:139675869 | G | T | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+1836C>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675869 | |||||||
| chr3:139675937 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-178+1768G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675937 | |||||||
| chr3:139675946 | A | T | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(78): Show |
85 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-178+1759T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139675946 | |||||||
| chr3:139676207 | T | C | 1 | a0001c0001t0001g0314 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-178+1498A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676207 | |||||||
| chr3:139676419 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+1286T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676419 | |||||||
| chr3:139676426 | A | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+1279T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676426 | |||||||
| chr3:139676439 | A | T | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(79): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-178+1266T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676439 | |||||||
| chr3:139676456 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-178+1249T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676456 | |||||||
| chr3:139676505 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-178+1200G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676505 | |||||||
| chr3:139676597 | G | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-178+1108C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676597 | |||||||
| chr3:139676632 | G | C | 78 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-178+1073C>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676632 | |||||||
| chr3:139676737 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-178+968T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676737 | |||||||
| chr3:139676849 | A | G | 22 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(19): Show |
22 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-178+856T>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676849 | |||||||
| chr3:139676943 | A | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-178+762T>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676943 | |||||||
| chr3:139676958 | T | C | 78 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-178+747A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139676958 | |||||||
| chr3:139677172 | T | G | 1 | a0001c0002t0001g0194 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-178+533A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677172 | |||||||
| chr3:139677320 | T | C | 234 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(231): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.-178+385A>G | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677320 | |||||||
| chr3:139677330 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-178+375G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677330 | |||||||
| chr3:139677547 | C | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0015 others(4): Show |
7 | HG01081.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+158G>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677547 | |||||||
| chr3:139677561 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0012 |
2 | HG01099.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-178+144G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677561 | |||||||
| chr3:139677608 | C | T | 12 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
12 | HG01109.hp1 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-178+97G>A | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677608 | |||||||
| chr3:139677620 | T | G | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(123): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-178+85A>C | NMNAT3 | ENSG00000163864.18 | transcript | ENST00000704800.1 | protein_coding | 1/6 | chr3 | 139677620 |