Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80018 |
| ensemblid | ENSG00000111300.10 |
| hgncid | 25783 |
| symbol | NAA25 |
| name | N-alpha-acetyltransferase 25, NatB auxiliary subunit |
| refseq_nuc | NM_024953.4 |
| refseq_prot | NP_079229.2 |
| ensembl_nuc | ENST00000261745.9 |
| ensembl_prot | ENSP00000261745.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 112026689 |
| end | 112108783 |
| strand | - |
| ver | v1.2 |
| region | chr12:112026689-112108783 |
| region5000 | chr12:112021689-112113783 |
| regionname0 | NAA25_chr12_112026689_112108783 |
| regionname5000 | NAA25_chr12_112021689_112113783 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 972 | 215 | 58 | 35 | 80 | 5 | 35 | 66 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| a0002 | 0/0 | 972 | 91 | 7 | 14 | 67 | 0 | 3 | 55 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| a0003 | 0/0 | 972 | 33 | 25 | 7 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| a0004 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| a0005 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| a0006 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | MATRG others(967): Show |
chr12 | 112021689 | 112113783 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2916 | 214 | 58 | 35 | 79 | 5 | 35 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0001c0006 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0002c0002 | 0/0 | 2916 | 87 | 7 | 14 | 63 | 0 | 3 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0002c0004 | 0/0 | 2916 | 4 | 0 | 0 | 4 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0003c0003 | 0/0 | 2916 | 33 | 25 | 7 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0004c0008 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0005c0007 | 0/0 | 2916 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 | ||
| a0006c0005 | 0/0 | 2916 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | ATGGC others(2911): Show |
chr12 | 112021689 | 112113783 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5771 | 110 | 13 | 30 | 34 | 4 | 28 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0003 | 0/0 | 5771 | 80 | 30 | 3 | 40 | 1 | 6 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0004 | 0/0 | 5771 | 6 | 5 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0005 | 0/0 | 5771 | 5 | 4 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0006 | 0/0 | 5771 | 4 | 0 | 0 | 4 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0007 | 0/0 | 5771 | 4 | 4 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0011 | 0/0 | 5771 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0012 | 0/1 | 5771 | 1 | 0 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0014 | 0/0 | 5771 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0015 | 0/0 | 5771 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0001t0016 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0001c0006t0001 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0002c0002t0002 | 0/0 | 5771 | 83 | 7 | 14 | 60 | 0 | 2 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0002c0002t0009 | 0/0 | 5771 | 2 | 0 | 0 | 2 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0002c0002t0010 | 0/0 | 5771 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0002c0002t0013 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0002c0004t0002 | 0/0 | 5771 | 4 | 0 | 0 | 4 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0003c0003t0001 | 0/0 | 5771 | 30 | 22 | 7 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0003c0003t0008 | 0/0 | 5770 | 3 | 3 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5765): Show |
chr12 | 112021689 | 112113783 |
| a0004c0008t0003 | 0/0 | 5771 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0005c0007t0003 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| a0006c0005t0017 | 0/0 | 5771 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | GCTTG others(5766): Show |
chr12 | 112021689 | 112113783 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0011g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0012g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0014g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0001c0006t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0009g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0010g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0002t0013g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0004t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0004t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0002c0004t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0003c0003t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0004c0008t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0005c0007t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| a0006c0005t0017g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0223 | EUR | GBR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | CHS | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | CHS | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0331 | EAS | CHS | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0254 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0303 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0304 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0302 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0222 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0080 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0207 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0206 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0226 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0145 | AMR | PUR | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0338 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0307 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0224 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0309 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0308 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01891 | hp1 | a0004 | c0008 | t0003 | g0021 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0305 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0329 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0265 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0322 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0325 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0204 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0330 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0326 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CDX | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0293 | EAS | CDX | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0006 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0291 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0209 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0210 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0036 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0225 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0079 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0089 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0124 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0253 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03017 | hp2 | a0002 | c0002 | t0010 | g0337 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03098 | hp1 | a0003 | c0003 | t0008 | g0103 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0235 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0121 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0119 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0003 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0300 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03453 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03516 | hp1 | a0003 | c0003 | t0008 | g0102 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | ESN | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0221 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0247 | AFR | GWD | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0233 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0120 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | CHB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0321 | EAS | CHB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0208 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18942 | hp2 | a0002 | c0004 | t0002 | g0297 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18959 | hp1 | a0002 | c0004 | t0002 | g0260 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18959 | hp2 | a0005 | c0007 | t0003 | g0022 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18967 | hp1 | a0002 | c0004 | t0002 | g0318 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18975 | hp2 | a0001 | c0006 | t0001 | g0150 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18981 | hp2 | a0002 | c0002 | t0009 | g0332 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19002 | hp2 | a0002 | c0004 | t0002 | g0301 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19043 | hp2 | a0003 | c0003 | t0008 | g0104 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19057 | hp1 | a0002 | c0002 | t0013 | g0319 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19063 | hp2 | a0002 | c0002 | t0009 | g0258 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19085 | hp1 | a0001 | c0001 | t0016 | g0156 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19240 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20129 | hp1 | a0006 | c0005 | t0017 | g0105 | AFR | ASW | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ASW | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | TSI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | TSI | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | GIH | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0314 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0090 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0248 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0246 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | MSL | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | USA | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | USA | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA21309 | hp1 | a0003 | c0003 | t0001 | g0256 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0125 | AFR | LWK | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0012 | g0201 | REF | REF | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0158 | REF | REF | NAA25_chr12_112021689_112113783 | NAA25 | chr12 | 112021689 | 112113783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112033286 | G | T | 1 | a0003 | 33 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(30): Show |
missense_variant | MODERATE | c.2743C>A | p.Leu915Ile | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/24 | 2753/5771 | 2743/2919 | 915/972 | chr12 | 112033286 | |||
| chr12:112039251 | T | C | 1 | a0002 | 91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
missense_variant | MODERATE | c.2627A>G | p.Lys876Arg | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/24 | 2637/5771 | 2627/2919 | 876/972 | chr12 | 112039251 | |||
| chr12:112042093 | C | G | 1 | a0005 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.2386G>C | p.Glu796Gln | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/24 | 2396/5771 | 2386/2919 | 796/972 | chr12 | 112042093 | |||
| chr12:112043088 | C | G | 1 | a0005 | 1 | NA18959.hp2 | missense_variant&splice_region_variant | MODERATE | c.2374G>C | p.Glu792Gln | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/24 | 2384/5771 | 2374/2919 | 792/972 | chr12 | 112043088 | |||
| chr12:112043180 | A | T | 1 | a0005 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.2282T>A | p.Met761Lys | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/24 | 2292/5771 | 2282/2919 | 761/972 | chr12 | 112043180 | |||
| chr12:112068960 | T | C | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1069A>G | p.Lys357Glu | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/24 | 1079/5771 | 1069/2919 | 357/972 | chr12 | 112068960 | |||
| chr12:112074717 | C | T | 1 | a0006 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.824G>A | p.Arg275Gln | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/24 | 834/5771 | 824/2919 | 275/972 | chr12 | 112074717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112048381 | G | A | 1 | a0004c0008 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1791C>T | p.Ile597Ile | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 16/24 | 1801/5771 | 1791/2919 | 597/972 | chr12 | 112048381 | |||
| chr12:112048393 | G | A | 1 | a0002c0004 | 4 | NA18942.hp2 NA18959.hp1 NA18967.hp1 others(1): Show |
synonymous_variant | LOW | c.1779C>T | p.Ile593Ile | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 16/24 | 1789/5771 | 1779/2919 | 593/972 | chr12 | 112048393 | |||
| chr12:112071959 | A | G | 1 | a0001c0006 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.972T>C | p.His324His | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/24 | 982/5771 | 972/2919 | 324/972 | chr12 | 112071959 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112026771 | G | C | 1 | a0002c0002t0013 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2760C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2760 | chr12 | 112026771 | ||||||
| chr12:112026827 | C | T | 5 | a0002c0002t0002 a0002c0002t0009 a0002c0002t0010 others(2): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2704G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2704 | chr12 | 112026827 | ||||||
| chr12:112026888 | A | G | 1 | a0001c0001t0006 | 4 | HG02027.hp1 NA18949.hp2 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2643T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2643 | chr12 | 112026888 | ||||||
| chr12:112026980 | T | C | 1 | a0001c0001t0014 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2551A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2551 | chr12 | 112026980 | ||||||
| chr12:112027089 | C | T | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(3): Show |
92 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2442G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2442 | chr12 | 112027089 | ||||||
| chr12:112027234 | G | A | 1 | a0001c0001t0007 | 4 | HG02965.hp1 HG03098.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2297C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2297 | chr12 | 112027234 | ||||||
| chr12:112027323 | A | T | 1 | a0001c0001t0001 | 2 | HG01978.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2208T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2208 | chr12 | 112027323 | ||||||
| chr12:112027324 | TA | T | 1 | a0003c0003t0008 | 3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2206delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2206 | chr12 | 112027324 | ||||||
| chr12:112027325 | A | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
157 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2206T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 2206 | chr12 | 112027325 | ||||||
| chr12:112028118 | G | C | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1413C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 1413 | chr12 | 112028118 | ||||||
| chr12:112028138 | A | C | 1 | a0001c0001t0011 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1393T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 1393 | chr12 | 112028138 | ||||||
| chr12:112028399 | A | C | 2 | a0001c0001t0004 a0006c0005t0017 |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1132T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 1132 | chr12 | 112028399 | ||||||
| chr12:112028663 | A | C | 1 | a0002c0002t0009 | 2 | NA18981.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*868T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 868 | chr12 | 112028663 | ||||||
| chr12:112028835 | G | C | 1 | a0001c0001t0016 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*696C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 696 | chr12 | 112028835 | ||||||
| chr12:112028960 | T | C | 1 | a0006c0005t0017 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 571 | chr12 | 112028960 | ||||||
| chr12:112029224 | C | T | 1 | a0002c0002t0010 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 307 | chr12 | 112029224 | ||||||
| chr12:112029524 | T | C | 1 | a0001c0001t0005 | 5 | HG01167.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 24/24 | 7 | chr12 | 112029524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:112030101 | T | C | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797-448A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030101 | |||||||
| chr12:112030210 | C | CA | 141 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0016 others(138): Show |
141 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.2797-558dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030210 | |||||||
| chr12:112030210 | C | CAA | 31 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(28): Show |
31 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.2797-559_2797-558d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030210 | |||||||
| chr12:112030210 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2797-568_2797-558d others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030210 | |||||||
| chr12:112030210 | CA | C | 10 | a0001c0001t0001g0185 a0001c0001t0004g0106 a0001c0001t0004g0114 others(7): Show |
10 | HG01099.hp2 HG01943.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.2797-558delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030210 | |||||||
| chr12:112030210 | CAA | C | 79 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(76): Show |
81 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.2797-559_2797-558d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030210 | |||||||
| chr12:112030402 | C | T | 25 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0262 others(22): Show |
27 | HG00544.hp2 HG02132.hp2 NA18747.hp1 others(24): Show |
intron_variant | MODIFIER | c.2797-749G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030402 | |||||||
| chr12:112030613 | C | T | 92 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(89): Show |
92 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(89): Show |
intron_variant | MODIFIER | c.2797-960G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030613 | |||||||
| chr12:112030635 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2797-982A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030635 | |||||||
| chr12:112030728 | T | C | 3 | a0002c0002t0002g0326 a0002c0002t0002g0327 a0002c0002t0002g0335 |
3 | HG02080.hp1 NA18961.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2797-1075A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030728 | |||||||
| chr12:112030940 | T | TA | 85 | a0001c0001t0001g0212 a0001c0001t0003g0019 a0001c0001t0003g0020 others(82): Show |
85 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(82): Show |
intron_variant | MODIFIER | c.2797-1288dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030940 | |||||||
| chr12:112030944 | A | AT | 128 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(125): Show |
130 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.2797-1292dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030944 | |||||||
| chr12:112030944 | A | T | 2 | a0001c0001t0016g0156 a0003c0003t0001g0254 |
2 | HG00733.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2797-1291T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030944 | |||||||
| chr12:112030944 | AT | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0173 a0001c0001t0001g0195 others(6): Show |
9 | HG01109.hp1 HG02451.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.2797-1292delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030944 | |||||||
| chr12:112030945 | T | A | 6 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0029 others(3): Show |
6 | HG01167.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2797-1292A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030945 | |||||||
| chr12:112030960 | A | T | 6 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0006t0001g0150 others(3): Show |
6 | HG02080.hp2 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2797-1307T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112030960 | |||||||
| chr12:112031080 | G | A | 1 | a0002c0002t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2797-1427C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031080 | |||||||
| chr12:112031273 | G | A | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797-1620C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031273 | |||||||
| chr12:112031288 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2797-1635C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031288 | |||||||
| chr12:112031351 | T | C | 13 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2797-1698A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031351 | |||||||
| chr12:112031576 | A | C | 1 | a0001c0001t0003g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2796+1657T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031576 | |||||||
| chr12:112031584 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2796+1649C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031584 | |||||||
| chr12:112031635 | G | A | 1 | a0002c0002t0002g0315 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2796+1598C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031635 | |||||||
| chr12:112031810 | T | C | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2796+1423A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031810 | |||||||
| chr12:112031867 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2796+1366G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112031867 | |||||||
| chr12:112032138 | G | T | 2 | a0001c0001t0003g0025 a0001c0001t0003g0026 |
2 | NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2796+1095C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112032138 | |||||||
| chr12:112032227 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2796+1006T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112032227 | |||||||
| chr12:112032299 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2796+934C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112032299 | |||||||
| chr12:112032346 | C | T | 1 | a0001c0001t0015g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2796+887G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112032346 | |||||||
| chr12:112032437 | G | A | 3 | a0001c0001t0003g0065 a0001c0001t0003g0066 a0001c0001t0003g0093 |
3 | HG02132.hp1 HG02523.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2796+796C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112032437 | |||||||
| chr12:112033021 | A | C | 3 | a0003c0003t0001g0206 a0003c0003t0001g0207 a0003c0003t0001g0210 |
3 | HG01168.hp1 HG01169.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2796+212T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112033021 | |||||||
| chr12:112033216 | T | A | 7 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(4): Show |
7 | HG02109.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2796+17A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 23/23 | chr12 | 112033216 | |||||||
| chr12:112033498 | T | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2650-119A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033498 | |||||||
| chr12:112033556 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2650-177G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033556 | |||||||
| chr12:112033598 | TA | T | 189 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(186): Show |
191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.2650-220delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033598 | |||||||
| chr12:112033722 | T | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2650-343A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033722 | |||||||
| chr12:112033854 | C | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2650-475G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033854 | |||||||
| chr12:112033912 | T | C | 3 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0226 |
3 | HG00099.hp2 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2650-533A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033912 | |||||||
| chr12:112033941 | CAT | C | 4 | a0001c0001t0005g0077 a0001c0001t0005g0078 a0001c0001t0005g0079 others(1): Show |
4 | HG02723.hp1 HG02818.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650-564_2650-563d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033941 | |||||||
| chr12:112033945 | T | C | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2650-566A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112033945 | |||||||
| chr12:112034281 | T | A | 4 | a0002c0004t0002g0260 a0002c0004t0002g0297 a0002c0004t0002g0301 others(1): Show |
4 | NA18942.hp2 NA18959.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650-902A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034281 | |||||||
| chr12:112034351 | C | T | 13 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(10): Show |
13 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2650-972G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034351 | |||||||
| chr12:112034363 | C | T | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650-984G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034363 | |||||||
| chr12:112034581 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2650-1202C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034581 | |||||||
| chr12:112034628 | A | AAAC | 95 | a0001c0001t0001g0122 a0001c0001t0001g0135 a0001c0001t0003g0033 others(92): Show |
97 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.2650-1252_2650-125 others(7): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034628 | |||||||
| chr12:112034628 | A | AAACAAC | 9 | a0001c0001t0003g0048 a0001c0001t0004g0106 a0001c0001t0004g0107 others(6): Show |
9 | HG01943.hp1 HG02129.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2650-1255_2650-125 others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034628 | |||||||
| chr12:112034811 | C | CA | 15 | a0001c0001t0001g0017 a0001c0001t0001g0200 a0001c0001t0001g0241 others(12): Show |
15 | HG01168.hp1 HG01169.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.2650-1433dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034811 | |||||||
| chr12:112034811 | C | CAA | 85 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(82): Show |
87 | HG00544.hp2 HG00735.hp1 HG01071.hp1 others(84): Show |
intron_variant | MODIFIER | c.2650-1434_2650-143 others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034811 | |||||||
| chr12:112034941 | G | A | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2650-1562C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112034941 | |||||||
| chr12:112035215 | C | CAAAAAAC others(327): Show |
1 | a0001c0001t0001g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2650-1837_2650-183 others(338): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035215 | |||||||
| chr12:112035321 | A | G | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2650-1942T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035321 | |||||||
| chr12:112035342 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2650-1963A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035342 | |||||||
| chr12:112035545 | G | A | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2650-2166C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035545 | |||||||
| chr12:112035681 | CT | C | 269 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(266): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.2650-2303delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035681 | |||||||
| chr12:112035693 | T | C | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2650-2314A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035693 | |||||||
| chr12:112035783 | T | G | 1 | a0002c0002t0002g0007 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2650-2404A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035783 | |||||||
| chr12:112035796 | G | A | 1 | a0002c0002t0002g0336 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2650-2417C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035796 | |||||||
| chr12:112035838 | T | C | 8 | a0003c0003t0001g0119 a0003c0003t0001g0222 a0003c0003t0001g0223 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.2650-2459A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035838 | |||||||
| chr12:112035917 | C | T | 2 | a0003c0003t0001g0120 a0003c0003t0001g0121 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2650-2538G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035917 | |||||||
| chr12:112035961 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2650-2582A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112035961 | |||||||
| chr12:112036293 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2650-2914G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036293 | |||||||
| chr12:112036319 | A | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02451.hp2 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2649+2910T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036319 | |||||||
| chr12:112036748 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0232 |
2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2649+2481G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036748 | |||||||
| chr12:112036753 | G | A | 1 | a0002c0002t0002g0294 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2649+2476C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036753 | |||||||
| chr12:112036840 | C | CA | 18 | a0001c0001t0001g0239 a0001c0001t0003g0033 a0001c0001t0003g0053 others(15): Show |
18 | HG01175.hp1 HG02132.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.2649+2388dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036840 | |||||||
| chr12:112036860 | C | G | 77 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0020 others(74): Show |
77 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.2649+2369G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036860 | |||||||
| chr12:112036914 | C | T | 1 | a0003c0003t0001g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2649+2315G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112036914 | |||||||
| chr12:112037056 | A | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2649+2173T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037056 | |||||||
| chr12:112037275 | C | CAT | 22 | a0001c0001t0001g0169 a0001c0001t0001g0174 a0001c0001t0001g0195 others(19): Show |
22 | HG00735.hp2 HG01109.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.2649+1952_2649+195 others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATAT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0155 a0001c0001t0001g0157 others(10): Show |
13 | HG00140.hp1 HG00544.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2649+1950_2649+195 others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATATAT | 6 | a0001c0001t0001g0113 a0001c0001t0001g0180 a0001c0001t0001g0185 others(3): Show |
6 | HG01071.hp2 HG01123.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2649+1948_2649+195 others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATATATA others(1): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0161 a0001c0001t0001g0172 |
3 | HG03239.hp1 NA19007.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2649+1946_2649+195 others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATATATA others(3): Show |
3 | a0001c0001t0001g0173 a0001c0001t0001g0177 a0001c0001t0001g0188 |
3 | HG02056.hp1 HG02976.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.2649+1944_2649+195 others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATATATA others(5): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0167 |
2 | HG00738.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2649+1942_2649+195 others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | C | CATATATA others(11): Show |
1 | a0001c0001t0003g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2649+1936_2649+195 others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CAT | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0147 a0001c0001t0001g0148 others(15): Show |
18 | HG01168.hp2 HG01243.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.2649+1952_2649+195 others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATAT | C | 51 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0136 others(48): Show |
51 | HG00140.hp2 HG00597.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.2649+1950_2649+195 others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATAT | C | 47 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0118 others(44): Show |
49 | HG00099.hp1 HG00544.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2649+1948_2649+195 others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(1): Show |
C | 53 | a0001c0001t0001g0014 a0001c0001t0001g0115 a0001c0001t0001g0131 others(50): Show |
53 | HG00733.hp1 HG01071.hp1 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.2649+1946_2649+195 others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(3): Show |
C | 23 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0127 others(20): Show |
23 | HG01123.hp1 HG01243.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.2649+1944_2649+195 others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(5): Show |
C | 17 | a0001c0001t0001g0151 a0001c0001t0001g0228 a0001c0001t0001g0230 others(14): Show |
17 | HG00597.hp2 HG01175.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.2649+1942_2649+195 others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(7): Show |
C | 7 | a0001c0001t0001g0112 a0001c0001t0001g0166 a0001c0001t0001g0232 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2649+1940_2649+195 others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(9): Show |
C | 2 | a0001c0001t0001g0241 a0001c0001t0003g0045 |
2 | HG01978.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2649+1938_2649+195 others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(11): Show |
C | 13 | a0001c0001t0003g0093 a0001c0001t0004g0106 a0001c0001t0004g0107 others(10): Show |
13 | HG01167.hp2 HG01943.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2649+1936_2649+195 others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(13): Show |
C | 12 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0026 others(9): Show |
12 | HG02145.hp1 HG02451.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2649+1934_2649+195 others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(15): Show |
C | 4 | a0001c0001t0003g0023 a0001c0001t0003g0031 a0001c0001t0003g0034 others(1): Show |
4 | HG01081.hp2 HG02258.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2649+1932_2649+195 others(26): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(21): Show |
C | 4 | a0001c0001t0003g0046 a0003c0003t0001g0120 a0003c0003t0001g0121 others(1): Show |
4 | HG01891.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2649+1926_2649+195 others(32): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(23): Show |
C | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0164 others(3): Show |
6 | HG02080.hp2 NA18955.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2649+1924_2649+195 others(34): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037275 | CATATATA others(25): Show |
C | 3 | a0003c0003t0001g0222 a0003c0003t0001g0223 a0003c0003t0001g0226 |
3 | HG00099.hp2 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2649+1922_2649+195 others(36): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037275 | |||||||
| chr12:112037331 | A | T | 7 | a0001c0001t0003g0044 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2649+1898T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037331 | |||||||
| chr12:112037459 | C | A | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2649+1770G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037459 | |||||||
| chr12:112037546 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2649+1683A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037546 | |||||||
| chr12:112037599 | T | C | 16 | a0001c0001t0003g0033 a0001c0001t0003g0053 a0001c0001t0003g0054 others(13): Show |
16 | HG02132.hp1 HG02523.hp1 NA18942.hp1 others(13): Show |
intron_variant | MODIFIER | c.2649+1630A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037599 | |||||||
| chr12:112037819 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2649+1410C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112037819 | |||||||
| chr12:112038104 | C | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0148 a0001c0001t0001g0153 others(2): Show |
5 | HG01255.hp1 HG01258.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2649+1125G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112038104 | |||||||
| chr12:112038851 | C | T | 1 | a0002c0002t0002g0261 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2649+378G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 22/23 | chr12 | 112038851 | |||||||
| chr12:112039429 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2539-90G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112039429 | |||||||
| chr12:112039655 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2539-316T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112039655 | |||||||
| chr12:112039709 | T | C | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2539-370A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112039709 | |||||||
| chr12:112039756 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2539-417A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112039756 | |||||||
| chr12:112039900 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2539-561G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112039900 | |||||||
| chr12:112040253 | A | C | 2 | a0002c0002t0002g0291 a0002c0002t0002g0314 |
2 | HG01123.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2538+228T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 21/23 | chr12 | 112040253 | |||||||
| chr12:112041053 | C | T | 3 | a0002c0002t0002g0298 a0002c0002t0002g0300 a0002c0002t0010g0337 |
3 | HG03017.hp2 HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2441-475G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041053 | |||||||
| chr12:112041054 | G | A | 2 | a0003c0003t0001g0206 a0003c0003t0001g0207 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2441-476C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041054 | |||||||
| chr12:112041068 | C | A | 97 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.2441-490G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041068 | |||||||
| chr12:112041128 | C | A | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2441-550G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041128 | |||||||
| chr12:112041158 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0152 a0001c0001t0001g0166 others(5): Show |
8 | HG03492.hp1 HG03669.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.2441-580T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041158 | |||||||
| chr12:112041191 | CTTT | C | 83 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0259 others(80): Show |
85 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.2441-616_2441-614d others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041191 | |||||||
| chr12:112041336 | C | T | 74 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0003g0034 others(71): Show |
74 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.2440+703G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041336 | |||||||
| chr12:112041457 | G | C | 1 | a0002c0002t0002g0290 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2440+582C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041457 | |||||||
| chr12:112041518 | A | C | 2 | a0002c0002t0002g0269 a0002c0002t0002g0270 |
2 | NA18948.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2440+521T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041518 | |||||||
| chr12:112041740 | C | T | 191 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(188): Show |
193 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.2440+299G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041740 | |||||||
| chr12:112041915 | C | T | 1 | a0001c0001t0015g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2440+124G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 20/23 | chr12 | 112041915 | |||||||
| chr12:112042423 | G | C | 1 | a0001c0001t0001g0339 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2375-319C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042423 | |||||||
| chr12:112042513 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2375-409A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042513 | |||||||
| chr12:112042515 | T | A | 18 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0002 others(15): Show |
18 | HG01175.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2375-411A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042515 | |||||||
| chr12:112042516 | T | A | 91 | a0001c0001t0003g0019 a0002c0002t0002g0001 a0002c0002t0002g0005 others(88): Show |
93 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.2375-412A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042516 | |||||||
| chr12:112042572 | T | C | 9 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2375-468A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042572 | |||||||
| chr12:112042886 | A | T | 1 | a0005c0007t0003g0022 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2374+202T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 19/23 | chr12 | 112042886 | |||||||
| chr12:112043280 | G | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2251-69C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 18/23 | chr12 | 112043280 | |||||||
| chr12:112043542 | C | T | 2 | a0002c0004t0002g0260 a0002c0004t0002g0318 |
2 | NA18959.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2250+83G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 18/23 | chr12 | 112043542 | |||||||
| chr12:112043928 | A | AT | 7 | a0001c0001t0001g0239 a0001c0001t0003g0025 a0001c0001t0003g0039 others(4): Show |
7 | HG01175.hp1 HG02145.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2007-61dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112043928 | |||||||
| chr12:112043967 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2007-99C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112043967 | |||||||
| chr12:112044002 | A | T | 1 | a0001c0001t0015g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2007-134T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044002 | |||||||
| chr12:112044021 | A | G | 97 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.2007-153T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044021 | |||||||
| chr12:112044119 | G | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0169 |
2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2007-251C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044119 | |||||||
| chr12:112044399 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2007-531C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044399 | |||||||
| chr12:112044466 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2007-598G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044466 | |||||||
| chr12:112044486 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2007-618G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044486 | |||||||
| chr12:112044668 | TCAAAACA others(3): Show |
T | 4 | a0001c0001t0001g0249 a0001c0001t0003g0213 a0001c0001t0003g0218 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2007-810_2007-801d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044668 | |||||||
| chr12:112044765 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2007-897C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044765 | |||||||
| chr12:112044875 | T | TA | 12 | a0001c0001t0001g0234 a0001c0001t0001g0239 a0001c0001t0003g0111 others(9): Show |
12 | HG01175.hp1 HG01943.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2007-1008dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044875 | |||||||
| chr12:112044913 | C | T | 1 | a0002c0002t0002g0300 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2007-1045G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112044913 | |||||||
| chr12:112045284 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0242 |
2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2007-1416C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045284 | |||||||
| chr12:112045366 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0003g0026 |
2 | NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2007-1498C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045366 | |||||||
| chr12:112045411 | C | T | 1 | a0003c0003t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2007-1543G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045411 | |||||||
| chr12:112045450 | G | A | 11 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(8): Show |
11 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2007-1582C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045450 | |||||||
| chr12:112045486 | CA | C | 31 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.2007-1619delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045486 | |||||||
| chr12:112045500 | A | AC | 77 | a0001c0001t0001g0212 a0001c0001t0001g0234 a0001c0001t0003g0020 others(74): Show |
77 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.2007-1633_2007-163 others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045500 | |||||||
| chr12:112045500 | A | C | 203 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(200): Show |
205 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(202): Show |
intron_variant | MODIFIER | c.2007-1632T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045500 | |||||||
| chr12:112045581 | G | A | 9 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2007-1713C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045581 | |||||||
| chr12:112045790 | G | C | 6 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2006+1875C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112045790 | |||||||
| chr12:112046455 | C | T | 1 | a0002c0002t0002g0315 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2006+1210G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112046455 | |||||||
| chr12:112046807 | A | G | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2006+858T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112046807 | |||||||
| chr12:112046834 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2006+831A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112046834 | |||||||
| chr12:112047229 | C | CT | 54 | a0001c0001t0001g0012 a0001c0001t0001g0185 a0001c0001t0001g0186 others(51): Show |
54 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.2006+435dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047229 | |||||||
| chr12:112047268 | G | C | 75 | a0001c0001t0001g0212 a0001c0001t0003g0020 a0001c0001t0003g0033 others(72): Show |
75 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.2006+397C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047268 | |||||||
| chr12:112047328 | T | C | 6 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2006+337A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047328 | |||||||
| chr12:112047390 | C | T | 2 | a0001c0001t0003g0045 a0001c0001t0003g0046 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2006+275G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047390 | |||||||
| chr12:112047530 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2006+135G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047530 | |||||||
| chr12:112047531 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2006+134G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 17/23 | chr12 | 112047531 | |||||||
| chr12:112048035 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1881-245G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 16/23 | chr12 | 112048035 | |||||||
| chr12:112048147 | G | A | 97 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1880+145C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 16/23 | chr12 | 112048147 | |||||||
| chr12:112048550 | T | G | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1729-107A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048550 | |||||||
| chr12:112048610 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1729-167G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048610 | |||||||
| chr12:112048649 | T | C | 3 | a0003c0003t0001g0037 a0003c0003t0001g0089 a0003c0003t0001g0090 |
3 | HG02109.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1729-206A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048649 | |||||||
| chr12:112048791 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1729-348A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048791 | |||||||
| chr12:112048874 | G | A | 6 | a0001c0001t0003g0054 a0001c0001t0003g0064 a0001c0001t0003g0083 others(3): Show |
6 | NA18946.hp2 NA18950.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1729-431C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048874 | |||||||
| chr12:112048991 | G | A | 7 | a0001c0001t0003g0044 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1729-548C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112048991 | |||||||
| chr12:112049014 | A | G | 19 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0157 others(16): Show |
19 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1729-571T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049014 | |||||||
| chr12:112049444 | T | C | 16 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(13): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1729-1001A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049444 | |||||||
| chr12:112049720 | G | A | 2 | a0001c0001t0003g0087 a0001c0001t0003g0099 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1729-1277C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049720 | |||||||
| chr12:112049731 | A | G | 3 | a0003c0003t0008g0102 a0003c0003t0008g0103 a0003c0003t0008g0104 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1729-1288T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049731 | |||||||
| chr12:112049832 | C | T | 1 | a0001c0001t0003g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1729-1389G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049832 | |||||||
| chr12:112049841 | T | C | 2 | a0002c0002t0002g0296 a0002c0002t0002g0299 |
2 | NA18943.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1729-1398A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049841 | |||||||
| chr12:112049986 | A | C | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1729-1543T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112049986 | |||||||
| chr12:112050029 | G | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1729-1586C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112050029 | |||||||
| chr12:112050047 | TA | T | 91 | a0001c0001t0001g0015 a0001c0001t0001g0173 a0001c0001t0003g0019 others(88): Show |
93 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1729-1605delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112050047 | |||||||
| chr12:112050319 | T | G | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1729-1876A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112050319 | |||||||
| chr12:112050663 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1729-2220G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112050663 | |||||||
| chr12:112050958 | T | C | 1 | a0001c0001t0005g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1729-2515A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112050958 | |||||||
| chr12:112051413 | G | A | 1 | a0002c0002t0002g0262 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1728+2145C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051413 | |||||||
| chr12:112051589 | C | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+1969G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051589 | |||||||
| chr12:112051593 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1728+1965T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051593 | |||||||
| chr12:112051668 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1728+1890G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051668 | |||||||
| chr12:112051686 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1728+1872T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051686 | |||||||
| chr12:112051717 | T | C | 92 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(89): Show |
92 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(89): Show |
intron_variant | MODIFIER | c.1728+1841A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051717 | |||||||
| chr12:112051771 | C | A | 1 | a0001c0001t0003g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1728+1787G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051771 | |||||||
| chr12:112051856 | T | G | 3 | a0001c0001t0004g0106 a0001c0001t0004g0108 a0001c0001t0004g0110 |
3 | HG01943.hp1 HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1728+1702A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112051856 | |||||||
| chr12:112052417 | G | A | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1728+1141C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112052417 | |||||||
| chr12:112052584 | C | A | 1 | a0002c0002t0002g0321 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1728+974G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112052584 | |||||||
| chr12:112052600 | GTTCAGA | G | 9 | a0003c0003t0001g0116 a0003c0003t0001g0119 a0003c0003t0001g0222 others(6): Show |
9 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1728+952_1728+957d others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112052600 | |||||||
| chr12:112052869 | G | A | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1728+689C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112052869 | |||||||
| chr12:112052960 | G | T | 226 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(223): Show |
228 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(225): Show |
intron_variant | MODIFIER | c.1728+598C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112052960 | |||||||
| chr12:112053072 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+486T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112053072 | |||||||
| chr12:112053181 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1728+377A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 15/23 | chr12 | 112053181 | |||||||
| chr12:112053821 | T | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1629-164A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 14/23 | chr12 | 112053821 | |||||||
| chr12:112053821 | T | TA | 145 | a0001c0001t0001g0012 a0001c0001t0001g0112 a0001c0001t0001g0115 others(142): Show |
145 | HG00140.hp2 HG00597.hp1 HG00733.hp1 others(142): Show |
intron_variant | MODIFIER | c.1629-165dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 14/23 | chr12 | 112053821 | |||||||
| chr12:112053821 | T | TAAA | 8 | a0001c0001t0003g0024 a0001c0001t0003g0027 a0001c0001t0003g0028 others(5): Show |
8 | HG02145.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1629-167_1629-165d others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 14/23 | chr12 | 112053821 | |||||||
| chr12:112053821 | TA | T | 96 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0001g0184 others(93): Show |
98 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.1629-165delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 14/23 | chr12 | 112053821 | |||||||
| chr12:112054666 | A | G | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-98T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112054666 | |||||||
| chr12:112054761 | A | T | 1 | a0001c0001t0003g0020 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1448-193T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112054761 | |||||||
| chr12:112054775 | C | A | 1 | a0001c0001t0014g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1448-207G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112054775 | |||||||
| chr12:112054919 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1448-351G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112054919 | |||||||
| chr12:112055069 | A | G | 8 | a0001c0001t0003g0048 a0001c0001t0003g0050 a0001c0001t0003g0052 others(5): Show |
8 | HG00597.hp1 HG02056.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-501T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055069 | |||||||
| chr12:112055076 | T | C | 1 | a0002c0004t0002g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1448-508A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055076 | |||||||
| chr12:112055079 | A | G | 2 | a0003c0003t0001g0246 a0003c0003t0001g0247 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1448-511T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055079 | |||||||
| chr12:112055263 | G | A | 189 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(186): Show |
191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.1448-695C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055263 | |||||||
| chr12:112055305 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1448-737A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055305 | |||||||
| chr12:112055325 | C | G | 1 | a0001c0001t0003g0053 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1448-757G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055325 | |||||||
| chr12:112055386 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1448-818C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055386 | |||||||
| chr12:112055486 | C | G | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1448-918G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055486 | |||||||
| chr12:112055520 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1448-952G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055520 | |||||||
| chr12:112055533 | A | G | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1448-965T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055533 | |||||||
| chr12:112055921 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1448-1353G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055921 | |||||||
| chr12:112055927 | T | A | 2 | a0002c0002t0002g0269 a0002c0002t0002g0270 |
2 | NA18948.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1448-1359A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055927 | |||||||
| chr12:112055984 | G | T | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1448-1416C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055984 | |||||||
| chr12:112055991 | G | C | 1 | a0003c0003t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1448-1423C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112055991 | |||||||
| chr12:112056211 | A | G | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1448-1643T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056211 | |||||||
| chr12:112056258 | C | A | 7 | a0001c0001t0003g0033 a0001c0001t0003g0054 a0001c0001t0003g0064 others(4): Show |
7 | NA18946.hp2 NA18950.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1448-1690G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056258 | |||||||
| chr12:112056337 | TA | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1448-1770delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056337 | |||||||
| chr12:112056374 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1448-1806T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056374 | |||||||
| chr12:112056521 | C | A | 8 | a0003c0003t0001g0119 a0003c0003t0001g0222 a0003c0003t0001g0223 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1448-1953G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056521 | |||||||
| chr12:112056648 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1448-2080G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056648 | |||||||
| chr12:112056911 | T | C | 1 | a0001c0001t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1448-2343A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056911 | |||||||
| chr12:112056964 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1448-2396G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112056964 | |||||||
| chr12:112057022 | T | C | 1 | a0003c0003t0001g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1448-2454A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057022 | |||||||
| chr12:112057048 | C | T | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1448-2480G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057048 | |||||||
| chr12:112057049 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1448-2481C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057049 | |||||||
| chr12:112057059 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1448-2491C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057059 | |||||||
| chr12:112057061 | G | A | 44 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(41): Show |
44 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1448-2493C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057061 | |||||||
| chr12:112057310 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1448-2742G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057310 | |||||||
| chr12:112057452 | T | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0197 |
3 | HG01106.hp2 HG01943.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1447+2818A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057452 | |||||||
| chr12:112057625 | C | T | 1 | a0003c0003t0001g0224 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1447+2645G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057625 | |||||||
| chr12:112057695 | A | C | 1 | a0001c0001t0004g0107 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1447+2575T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057695 | |||||||
| chr12:112057958 | C | T | 1 | a0002c0002t0002g0286 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1447+2312G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112057958 | |||||||
| chr12:112058680 | T | C | 9 | a0001c0001t0003g0019 a0001c0001t0003g0044 a0001c0001t0003g0072 others(6): Show |
9 | HG01081.hp1 HG01099.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447+1590A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112058680 | |||||||
| chr12:112058813 | C | T | 10 | a0003c0003t0001g0116 a0003c0003t0001g0119 a0003c0003t0001g0145 others(7): Show |
10 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1447+1457G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112058813 | |||||||
| chr12:112059075 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1447+1184_1447+119 others(15): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAA | C | 13 | a0001c0001t0001g0135 a0001c0001t0001g0147 a0001c0001t0001g0148 others(10): Show |
13 | HG00733.hp2 HG00735.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1447+1189_1447+119 others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
25 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.1447+1188_1447+119 others(11): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(1): Show |
C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0118 a0001c0001t0001g0129 others(25): Show |
28 | HG00140.hp1 HG00738.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1447+1187_1447+119 others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(2): Show |
C | 18 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0153 others(15): Show |
18 | HG01243.hp2 HG01258.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447+1186_1447+119 others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0189 a0001c0006t0001g0150 others(2): Show |
5 | HG02886.hp2 NA18955.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447+1185_1447+119 others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(5): Show |
C | 6 | a0001c0001t0001g0172 a0001c0001t0001g0251 a0003c0003t0001g0035 others(3): Show |
6 | HG02559.hp1 HG02630.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447+1183_1447+119 others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0115 a0003c0003t0001g0116 |
2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1447+1182_1447+119 others(17): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(8): Show |
C | 3 | a0003c0003t0001g0224 a0003c0003t0001g0226 a0003c0003t0001g0256 |
3 | HG01175.hp2 HG01361.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1447+1180_1447+119 others(19): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0177 a0003c0003t0001g0119 a0003c0003t0001g0222 others(3): Show |
6 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1447+1179_1447+119 others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0241 |
2 | HG01978.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1447+1175_1447+119 others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1447+1174_1447+119 others(25): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0001g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1447+1173_1447+119 others(26): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(16): Show |
C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0242 |
2 | HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1447+1172_1447+119 others(27): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(17): Show |
C | 4 | a0001c0001t0001g0184 a0003c0003t0001g0204 a0003c0003t0001g0207 others(1): Show |
4 | HG01168.hp1 HG02055.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447+1171_1447+119 others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(18): Show |
C | 6 | a0001c0001t0001g0211 a0003c0003t0001g0203 a0003c0003t0001g0205 others(3): Show |
6 | HG01169.hp2 HG02572.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1447+1170_1447+119 others(29): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(19): Show |
C | 3 | a0001c0001t0001g0237 a0001c0001t0001g0249 a0001c0001t0004g0114 |
3 | HG03927.hp1 NA19030.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1447+1169_1447+119 others(30): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(20): Show |
C | 7 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447+1168_1447+119 others(31): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(21): Show |
C | 11 | a0001c0001t0011g0253 a0002c0002t0002g0288 a0002c0002t0002g0296 others(8): Show |
11 | HG00544.hp2 HG00735.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447+1167_1447+119 others(32): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(22): Show |
C | 78 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(75): Show |
80 | HG00597.hp2 HG01071.hp1 HG01081.hp2 others(77): Show |
intron_variant | MODIFIER | c.1447+1166_1447+119 others(33): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(23): Show |
C | 3 | a0001c0001t0001g0190 a0002c0004t0002g0318 a0003c0003t0001g0248 |
3 | HG01433.hp2 HG02486.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1447+1165_1447+119 others(34): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(27): Show |
C | 1 | a0001c0001t0003g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1447+1161_1447+119 others(38): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059075 | CAAAAAAA others(28): Show |
C | 91 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(88): Show |
91 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(88): Show |
intron_variant | MODIFIER | c.1447+1160_1447+119 others(39): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059075 | |||||||
| chr12:112059100 | A | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0176 |
2 | NA19079.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1447+1170T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059100 | |||||||
| chr12:112059102 | A | C | 1 | a0001c0001t0001g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1447+1168T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059102 | |||||||
| chr12:112059107 | A | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0167 a0001c0001t0001g0173 others(3): Show |
6 | NA18941.hp2 NA18948.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.1447+1163T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059107 | |||||||
| chr12:112059111 | A | C | 4 | a0001c0001t0001g0167 a0001c0001t0001g0173 a0001c0001t0001g0176 others(1): Show |
4 | NA18948.hp1 NA19002.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447+1159T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059111 | |||||||
| chr12:112059112 | A | C | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1447+1158T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059112 | |||||||
| chr12:112059316 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1447+954G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059316 | |||||||
| chr12:112059341 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1447+929G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059341 | |||||||
| chr12:112059600 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1447+670A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059600 | |||||||
| chr12:112059810 | G | GT | 125 | a0001c0001t0001g0122 a0001c0001t0001g0165 a0001c0001t0001g0178 others(122): Show |
127 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.1447+459dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059810 | |||||||
| chr12:112059831 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1447+439C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059831 | |||||||
| chr12:112059903 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1447+367C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059903 | |||||||
| chr12:112059994 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1447+276C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059994 | |||||||
| chr12:112059996 | C | T | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1447+274G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112059996 | |||||||
| chr12:112060099 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1447+171C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 13/23 | chr12 | 112060099 | |||||||
| chr12:112060486 | A | T | 1 | a0003c0003t0008g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1358-127T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 12/23 | chr12 | 112060486 | |||||||
| chr12:112060647 | A | G | 1 | a0001c0001t0003g0215 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1358-288T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 12/23 | chr12 | 112060647 | |||||||
| chr12:112061779 | A | T | 97 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1150-391T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112061779 | |||||||
| chr12:112062053 | C | T | 83 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0259 others(80): Show |
85 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1150-665G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062053 | |||||||
| chr12:112062365 | C | T | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1150-977G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062365 | |||||||
| chr12:112062400 | CA | C | 12 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0002c0002t0002g0325 others(9): Show |
12 | HG01168.hp1 HG01169.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150-1013delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062400 | |||||||
| chr12:112062450 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1150-1062G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062450 | |||||||
| chr12:112062543 | A | G | 1 | a0002c0002t0002g0300 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1150-1155T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062543 | |||||||
| chr12:112062756 | T | G | 1 | a0001c0001t0006g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1150-1368A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062756 | |||||||
| chr12:112062883 | A | C | 78 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(75): Show |
78 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(75): Show |
intron_variant | MODIFIER | c.1150-1495T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112062883 | |||||||
| chr12:112063059 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1150-1671G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063059 | |||||||
| chr12:112063112 | T | TAAAAATC others(315): Show |
1 | a0003c0003t0001g0037 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1150-1725_1150-172 others(326): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063112 | |||||||
| chr12:112063112 | T | TAAAAATC others(329): Show |
1 | a0003c0003t0001g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1150-1725_1150-172 others(340): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063112 | |||||||
| chr12:112063112 | T | TAAAAATC others(330): Show |
1 | a0003c0003t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1150-1725_1150-172 others(341): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063112 | |||||||
| chr12:112063191 | A | G | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1150-1803T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063191 | |||||||
| chr12:112063213 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150-1825G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063213 | |||||||
| chr12:112063304 | G | T | 1 | a0001c0001t0003g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1150-1916C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063304 | |||||||
| chr12:112063433 | G | A | 91 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(88): Show |
91 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(88): Show |
intron_variant | MODIFIER | c.1150-2045C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063433 | |||||||
| chr12:112063722 | A | T | 98 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(95): Show |
100 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.1150-2334T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063722 | |||||||
| chr12:112063827 | T | G | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-2439A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063827 | |||||||
| chr12:112063879 | T | C | 1 | a0002c0002t0002g0290 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1150-2491A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063879 | |||||||
| chr12:112063903 | C | G | 1 | a0002c0002t0002g0286 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1150-2515G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063903 | |||||||
| chr12:112063962 | T | G | 226 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(223): Show |
228 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(225): Show |
intron_variant | MODIFIER | c.1150-2574A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112063962 | |||||||
| chr12:112064053 | A | G | 1 | a0003c0003t0001g0203 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1150-2665T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064053 | |||||||
| chr12:112064249 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0176 |
2 | NA19079.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1150-2861C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064249 | |||||||
| chr12:112064295 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1150-2907C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064295 | |||||||
| chr12:112064303 | G | A | 7 | a0001c0001t0003g0044 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-2915C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064303 | |||||||
| chr12:112064319 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1150-2931C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064319 | |||||||
| chr12:112064603 | A | G | 1 | a0001c0001t0005g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1150-3215T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064603 | |||||||
| chr12:112064634 | A | G | 269 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(266): Show |
271 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(268): Show |
intron_variant | MODIFIER | c.1150-3246T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064634 | |||||||
| chr12:112064847 | G | A | 1 | a0002c0002t0002g0325 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1150-3459C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064847 | |||||||
| chr12:112064990 | C | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG01255.hp1 HG01496.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-3602G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112064990 | |||||||
| chr12:112065497 | CA | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG01256.hp2 NA18960.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1149+3382delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065497 | |||||||
| chr12:112065521 | G | A | 2 | a0003c0003t0001g0246 a0003c0003t0001g0247 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1149+3359C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065521 | |||||||
| chr12:112065641 | C | T | 7 | a0001c0001t0001g0152 a0001c0001t0001g0166 a0001c0001t0001g0172 others(4): Show |
7 | HG03492.hp1 HG03710.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149+3239G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065641 | |||||||
| chr12:112065670 | T | A | 92 | a0001c0001t0001g0212 a0001c0001t0003g0019 a0001c0001t0003g0020 others(89): Show |
92 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(89): Show |
intron_variant | MODIFIER | c.1149+3210A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065670 | |||||||
| chr12:112065723 | A | C | 3 | a0001c0001t0003g0069 a0001c0001t0003g0087 a0001c0001t0003g0099 |
3 | HG02055.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1149+3157T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065723 | |||||||
| chr12:112065789 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1149+3091C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065789 | |||||||
| chr12:112065873 | G | A | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1149+3007C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065873 | |||||||
| chr12:112065905 | C | A | 2 | a0003c0003t0008g0102 a0003c0003t0008g0104 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1149+2975G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065905 | |||||||
| chr12:112065923 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1149+2957T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112065923 | |||||||
| chr12:112066179 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1149+2701C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112066179 | |||||||
| chr12:112066501 | CCT | C | 92 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(89): Show |
92 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(89): Show |
intron_variant | MODIFIER | c.1149+2377_1149+237 others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112066501 | |||||||
| chr12:112066574 | C | A | 1 | a0002c0002t0002g0270 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1149+2306G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112066574 | |||||||
| chr12:112067186 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149+1694C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067186 | |||||||
| chr12:112067219 | A | C | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149+1661T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067219 | |||||||
| chr12:112067232 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1149+1648T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067232 | |||||||
| chr12:112067372 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1149+1508A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067372 | |||||||
| chr12:112067378 | T | A | 227 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(224): Show |
229 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(226): Show |
intron_variant | MODIFIER | c.1149+1502A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067378 | |||||||
| chr12:112067506 | C | T | 1 | a0002c0002t0002g0304 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1149+1374G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112067506 | |||||||
| chr12:112068052 | T | C | 1 | a0003c0003t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1149+828A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068052 | |||||||
| chr12:112068142 | G | A | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1149+738C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068142 | |||||||
| chr12:112068145 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1149+735G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068145 | |||||||
| chr12:112068180 | C | T | 8 | a0003c0003t0001g0119 a0003c0003t0001g0222 a0003c0003t0001g0223 others(5): Show |
8 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149+700G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068180 | |||||||
| chr12:112068187 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1149+693C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068187 | |||||||
| chr12:112068194 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1149+686G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068194 | |||||||
| chr12:112068206 | T | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0032 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1149+674A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 11/23 | chr12 | 112068206 | |||||||
| chr12:112069052 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1037-60C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069052 | |||||||
| chr12:112069296 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1037-304C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069296 | |||||||
| chr12:112069301 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1037-309A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069301 | |||||||
| chr12:112069757 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1037-765A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069757 | |||||||
| chr12:112069928 | G | C | 1 | a0002c0002t0002g0290 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1037-936C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069928 | |||||||
| chr12:112069997 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1037-1005C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069997 | |||||||
| chr12:112069998 | A | C | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.1037-1006T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112069998 | |||||||
| chr12:112070262 | T | C | 1 | a0002c0002t0010g0337 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1037-1270A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070262 | |||||||
| chr12:112070413 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1037-1421A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070413 | |||||||
| chr12:112070603 | G | A | 33 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(30): Show |
33 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1036+1292C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070603 | |||||||
| chr12:112070620 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1036+1275C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070620 | |||||||
| chr12:112070630 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1036+1265A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070630 | |||||||
| chr12:112070632 | C | T | 9 | a0001c0001t0001g0180 a0003c0003t0001g0203 a0003c0003t0001g0204 others(6): Show |
9 | HG01071.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1036+1263G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070632 | |||||||
| chr12:112070638 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1036+1257G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070638 | |||||||
| chr12:112070895 | T | C | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.1036+1000A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070895 | |||||||
| chr12:112070896 | G | A | 2 | a0002c0002t0009g0258 a0002c0002t0009g0332 |
2 | NA18981.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1036+999C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070896 | |||||||
| chr12:112070989 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1036+906G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112070989 | |||||||
| chr12:112071003 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1036+892A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071003 | |||||||
| chr12:112071071 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1036+824G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071071 | |||||||
| chr12:112071256 | G | A | 189 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(186): Show |
191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.1036+639C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071256 | |||||||
| chr12:112071328 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1036+567A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071328 | |||||||
| chr12:112071477 | G | A | 77 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0020 others(74): Show |
77 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.1036+418C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071477 | |||||||
| chr12:112071539 | C | T | 2 | a0002c0002t0002g0259 a0002c0002t0002g0321 |
2 | NA18747.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1036+356G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071539 | |||||||
| chr12:112071873 | A | C | 97 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1036+22T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 10/23 | chr12 | 112071873 | |||||||
| chr12:112072080 | T | C | 1 | a0002c0002t0002g0312 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.867-16A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072080 | |||||||
| chr12:112072196 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.867-132C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072196 | |||||||
| chr12:112072460 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.867-396G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072460 | |||||||
| chr12:112072466 | G | A | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.867-402C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072466 | |||||||
| chr12:112072469 | C | T | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.867-405G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072469 | |||||||
| chr12:112072600 | T | C | 269 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(266): Show |
271 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(268): Show |
intron_variant | MODIFIER | c.867-536A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072600 | |||||||
| chr12:112072608 | C | CA | 90 | a0001c0001t0003g0047 a0002c0002t0002g0001 a0002c0002t0002g0005 others(87): Show |
92 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.867-545dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072608 | |||||||
| chr12:112072628 | GA | G | 91 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(88): Show |
93 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.867-565delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072628 | |||||||
| chr12:112072710 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.867-646C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112072710 | |||||||
| chr12:112073054 | T | C | 1 | a0006c0005t0017g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.867-990A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073054 | |||||||
| chr12:112073154 | G | T | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.867-1090C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073154 | |||||||
| chr12:112073261 | T | TAC | 35 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0147 others(32): Show |
35 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.867-1199_867-1198d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073261 | |||||||
| chr12:112073261 | T | TACAC | 4 | a0001c0001t0006g0057 a0001c0001t0006g0094 a0003c0003t0008g0102 others(1): Show |
4 | HG03516.hp1 NA18949.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.867-1201_867-1198d others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073261 | |||||||
| chr12:112073261 | TAC | T | 97 | a0001c0001t0001g0211 a0001c0001t0001g0249 a0001c0001t0003g0111 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.867-1199_867-1198d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073261 | |||||||
| chr12:112073263 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.867-1199G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073263 | |||||||
| chr12:112073288 | A | G | 1 | a0003c0003t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.867-1224T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073288 | |||||||
| chr12:112073363 | A | G | 16 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(13): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.867-1299T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073363 | |||||||
| chr12:112073431 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.866+1244C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073431 | |||||||
| chr12:112073476 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866+1199C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073476 | |||||||
| chr12:112073677 | C | A | 1 | a0001c0001t0016g0156 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.866+998G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073677 | |||||||
| chr12:112073731 | C | G | 1 | a0001c0001t0001g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.866+944G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073731 | |||||||
| chr12:112073852 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.866+823C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073852 | |||||||
| chr12:112073923 | A | G | 3 | a0001c0001t0001g0122 a0003c0003t0001g0120 a0003c0003t0001g0121 |
3 | HG02970.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.866+752T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112073923 | |||||||
| chr12:112074040 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.866+635T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074040 | |||||||
| chr12:112074109 | G | C | 25 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0262 others(22): Show |
27 | HG00544.hp2 HG02132.hp2 NA18747.hp1 others(24): Show |
intron_variant | MODIFIER | c.866+566C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074109 | |||||||
| chr12:112074277 | G | C | 93 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(90): Show |
93 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(90): Show |
intron_variant | MODIFIER | c.866+398C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074277 | |||||||
| chr12:112074341 | C | CA | 34 | a0001c0001t0001g0122 a0001c0001t0001g0167 a0001c0001t0001g0178 others(31): Show |
34 | HG00733.hp1 HG01106.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.866+333dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074341 | |||||||
| chr12:112074341 | C | CAAAA | 73 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0007 others(70): Show |
75 | HG00544.hp2 HG01071.hp1 HG01123.hp1 others(72): Show |
intron_variant | MODIFIER | c.866+330_866+333dup others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074341 | |||||||
| chr12:112074341 | C | CAAAAA | 12 | a0002c0002t0002g0005 a0002c0002t0002g0262 a0002c0002t0002g0274 others(9): Show |
12 | HG00597.hp2 HG00735.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.866+329_866+333dup others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074341 | |||||||
| chr12:112074341 | CA | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0134 others(7): Show |
10 | HG01928.hp1 HG02148.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.866+333delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074341 | |||||||
| chr12:112074341 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.866+321_866+333del others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074341 | |||||||
| chr12:112074464 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.866+211A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 9/23 | chr12 | 112074464 | |||||||
| chr12:112074835 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.777-71A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112074835 | |||||||
| chr12:112074896 | T | G | 8 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.777-132A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112074896 | |||||||
| chr12:112075141 | G | A | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.777-377C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112075141 | |||||||
| chr12:112075250 | A | G | 1 | a0003c0003t0001g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.776+428T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112075250 | |||||||
| chr12:112075314 | G | A | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.776+364C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112075314 | |||||||
| chr12:112075458 | G | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0004 |
2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.776+220C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112075458 | |||||||
| chr12:112075557 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.776+121G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 8/23 | chr12 | 112075557 | |||||||
| chr12:112075853 | G | A | 4 | a0002c0002t0002g0302 a0002c0002t0002g0303 a0002c0002t0002g0308 others(1): Show |
4 | HG00735.hp1 HG01081.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-64C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112075853 | |||||||
| chr12:112075869 | G | A | 1 | a0003c0003t0001g0246 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.665-80C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112075869 | |||||||
| chr12:112075941 | G | A | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-152C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112075941 | |||||||
| chr12:112076178 | C | T | 1 | a0001c0001t0006g0094 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.665-389G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076178 | |||||||
| chr12:112076205 | A | G | 1 | a0002c0002t0009g0332 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.665-416T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076205 | |||||||
| chr12:112076328 | A | T | 22 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(19): Show |
22 | HG01993.hp1 HG02135.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.665-539T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076328 | |||||||
| chr12:112076329 | G | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.665-540C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076329 | |||||||
| chr12:112076362 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0255 |
2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.665-573A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076362 | |||||||
| chr12:112076597 | T | G | 1 | a0002c0002t0002g0314 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.665-808A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076597 | |||||||
| chr12:112076690 | T | G | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.665-901A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076690 | |||||||
| chr12:112076998 | A | C | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+1190T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112076998 | |||||||
| chr12:112077015 | A | AC | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.664+1172_664+1173i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077015 | |||||||
| chr12:112077095 | G | C | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+1093C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077095 | |||||||
| chr12:112077119 | G | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1069C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077119 | |||||||
| chr12:112077131 | A | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+1057T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077131 | |||||||
| chr12:112077179 | T | A | 42 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(39): Show |
42 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.664+1009A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077179 | |||||||
| chr12:112077273 | A | G | 268 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(265): Show |
270 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(267): Show |
intron_variant | MODIFIER | c.664+915T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077273 | |||||||
| chr12:112077342 | G | A | 22 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(19): Show |
22 | HG01993.hp1 HG02135.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.664+846C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077342 | |||||||
| chr12:112077472 | C | CA | 14 | a0001c0001t0001g0013 a0001c0001t0003g0023 a0001c0001t0003g0024 others(11): Show |
14 | HG02145.hp1 HG02148.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.664+715dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077472 | |||||||
| chr12:112077472 | C | CAAAA | 96 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(93): Show |
98 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.664+712_664+715dup others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077472 | |||||||
| chr12:112077508 | G | T | 74 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0003g0034 others(71): Show |
74 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.664+680C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077508 | |||||||
| chr12:112077526 | G | A | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+662C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077526 | |||||||
| chr12:112077565 | C | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.664+623G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077565 | |||||||
| chr12:112077598 | A | C | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.664+590T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077598 | |||||||
| chr12:112077620 | T | C | 1 | a0002c0004t0002g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.664+568A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077620 | |||||||
| chr12:112077780 | T | C | 1 | a0002c0002t0010g0337 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.664+408A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077780 | |||||||
| chr12:112077801 | T | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.664+387A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077801 | |||||||
| chr12:112077973 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0232 |
2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.664+215G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112077973 | |||||||
| chr12:112078003 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.664+185C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112078003 | |||||||
| chr12:112078108 | T | C | 75 | a0001c0001t0001g0212 a0001c0001t0003g0020 a0001c0001t0003g0033 others(72): Show |
75 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.664+80A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 7/23 | chr12 | 112078108 | |||||||
| chr12:112078789 | C | T | 1 | a0002c0002t0010g0337 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.478-48G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112078789 | |||||||
| chr12:112078833 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.478-92A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112078833 | |||||||
| chr12:112078879 | G | A | 5 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-138C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112078879 | |||||||
| chr12:112079028 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.478-287G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112079028 | |||||||
| chr12:112079323 | A | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.478-582T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112079323 | |||||||
| chr12:112079406 | A | G | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.478-665T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112079406 | |||||||
| chr12:112079464 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.478-723C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112079464 | |||||||
| chr12:112079838 | T | C | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.478-1097A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112079838 | |||||||
| chr12:112080001 | C | G | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+1059G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080001 | |||||||
| chr12:112080046 | C | T | 1 | a0002c0002t0002g0333 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.477+1014G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080046 | |||||||
| chr12:112080066 | G | GTCGGGAG others(23): Show |
1 | a0002c0002t0009g0332 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.477+993_477+994ins others(30): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080066 | |||||||
| chr12:112080071 | G | A | 5 | a0001c0001t0005g0077 a0001c0001t0005g0078 a0001c0001t0005g0079 others(2): Show |
5 | HG01167.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+989C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080071 | |||||||
| chr12:112080263 | A | G | 1 | a0002c0002t0010g0337 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.477+797T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080263 | |||||||
| chr12:112080278 | C | CA | 27 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0127 others(24): Show |
27 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.477+781dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080278 | |||||||
| chr12:112080278 | CA | C | 28 | a0001c0001t0003g0019 a0001c0001t0003g0023 a0001c0001t0003g0024 others(25): Show |
28 | HG01928.hp2 HG01943.hp1 HG02135.hp2 others(25): Show |
intron_variant | MODIFIER | c.477+781delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080278 | |||||||
| chr12:112080278 | CAA | C | 78 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0002c0002t0002g0001 others(75): Show |
80 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.477+780_477+781del others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080278 | |||||||
| chr12:112080294 | A | C | 65 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0003g0034 others(62): Show |
65 | HG00597.hp1 HG01167.hp2 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.477+766T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080294 | |||||||
| chr12:112080394 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+666T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080394 | |||||||
| chr12:112080396 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+664T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080396 | |||||||
| chr12:112080397 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+663A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080397 | |||||||
| chr12:112080399 | C | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+661G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080399 | |||||||
| chr12:112080400 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+660T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080400 | |||||||
| chr12:112080402 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+658T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080402 | |||||||
| chr12:112080404 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+656C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080404 | |||||||
| chr12:112080405 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+655G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080405 | |||||||
| chr12:112080406 | T | G | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+654A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080406 | |||||||
| chr12:112080409 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+651A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080409 | |||||||
| chr12:112080412 | C | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+648G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080412 | |||||||
| chr12:112080416 | A | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+644T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080416 | |||||||
| chr12:112080419 | C | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+641G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080419 | |||||||
| chr12:112080420 | C | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+640G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080420 | |||||||
| chr12:112080439 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+621T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080439 | |||||||
| chr12:112080440 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+620C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080440 | |||||||
| chr12:112080442 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+618G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080442 | |||||||
| chr12:112080443 | A | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+617T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080443 | |||||||
| chr12:112080444 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+616C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080444 | |||||||
| chr12:112080446 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+614T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080446 | |||||||
| chr12:112080447 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+613C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080447 | |||||||
| chr12:112080451 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+609A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080451 | |||||||
| chr12:112080456 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+604C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080456 | |||||||
| chr12:112080457 | A | G | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+603T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080457 | |||||||
| chr12:112080465 | A | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+595T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080465 | |||||||
| chr12:112080466 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+594C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080466 | |||||||
| chr12:112080470 | A | G | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+590T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080470 | |||||||
| chr12:112080473 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+587T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080473 | |||||||
| chr12:112080476 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+584T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080476 | |||||||
| chr12:112080477 | G | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+583C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080477 | |||||||
| chr12:112080485 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+575T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080485 | |||||||
| chr12:112080492 | T | C | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.477+568A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080492 | |||||||
| chr12:112080493 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+567C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080493 | |||||||
| chr12:112080494 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+566T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080494 | |||||||
| chr12:112080496 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+564T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080496 | |||||||
| chr12:112080501 | G | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+559C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080501 | |||||||
| chr12:112080507 | A | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+553T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080507 | |||||||
| chr12:112080539 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+521A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080539 | |||||||
| chr12:112080540 | C | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+520G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080540 | |||||||
| chr12:112080541 | G | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+519C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080541 | |||||||
| chr12:112080570 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+490C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080570 | |||||||
| chr12:112080582 | C | G | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+478G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080582 | |||||||
| chr12:112080584 | T | C | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+476A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080584 | |||||||
| chr12:112080587 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+473C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080587 | |||||||
| chr12:112080593 | T | A | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+467A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080593 | |||||||
| chr12:112080596 | G | T | 1 | a0001c0001t0003g0059 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.477+464C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080596 | |||||||
| chr12:112080677 | T | C | 1 | a0001c0001t0003g0025 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.477+383A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080677 | |||||||
| chr12:112080741 | C | T | 8 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.477+319G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080741 | |||||||
| chr12:112080999 | G | A | 47 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0259 others(44): Show |
49 | HG00544.hp2 HG01123.hp1 HG02071.hp2 others(46): Show |
intron_variant | MODIFIER | c.477+61C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 5/23 | chr12 | 112080999 | |||||||
| chr12:112081591 | T | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.403-457A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112081591 | |||||||
| chr12:112081912 | G | A | 1 | a0001c0001t0003g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.403-778C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112081912 | |||||||
| chr12:112081935 | T | C | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.403-801A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112081935 | |||||||
| chr12:112081960 | A | C | 5 | a0001c0001t0001g0147 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG00099.hp1 HG01168.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-826T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112081960 | |||||||
| chr12:112082013 | G | T | 1 | a0001c0001t0001g0234 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403-879C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082013 | |||||||
| chr12:112082434 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0011g0253 a0004c0008t0003g0021 |
3 | HG01891.hp1 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.403-1300C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082434 | |||||||
| chr12:112082708 | A | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-1574T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082708 | |||||||
| chr12:112082786 | C | G | 1 | a0002c0002t0002g0271 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.403-1652G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082786 | |||||||
| chr12:112082787 | G | C | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.403-1653C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082787 | |||||||
| chr12:112082802 | C | CG | 5 | a0001c0001t0001g0228 a0001c0001t0001g0241 a0001c0001t0001g0251 others(2): Show |
5 | HG01099.hp2 HG01978.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-1669dupC | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082802 | |||||||
| chr12:112082803 | G | A | 1 | a0003c0003t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.403-1669C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082803 | |||||||
| chr12:112082987 | G | C | 7 | a0001c0001t0003g0044 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-1853C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082987 | |||||||
| chr12:112082988 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.403-1854C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112082988 | |||||||
| chr12:112083035 | C | T | 1 | a0002c0002t0002g0290 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.403-1901G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083035 | |||||||
| chr12:112083079 | C | T | 268 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(265): Show |
270 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(267): Show |
intron_variant | MODIFIER | c.403-1945G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083079 | |||||||
| chr12:112083217 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-2083G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083217 | |||||||
| chr12:112083321 | A | G | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-2187T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083321 | |||||||
| chr12:112083440 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.403-2306C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083440 | |||||||
| chr12:112083479 | G | C | 1 | a0001c0001t0006g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.403-2345C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083479 | |||||||
| chr12:112083553 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.403-2419C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083553 | |||||||
| chr12:112083598 | G | A | 1 | a0001c0001t0003g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.403-2464C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083598 | |||||||
| chr12:112083644 | G | A | 269 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(266): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.403-2510C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083644 | |||||||
| chr12:112083927 | A | G | 1 | a0003c0003t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.403-2793T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083927 | |||||||
| chr12:112083959 | C | T | 1 | a0001c0001t0003g0026 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.403-2825G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112083959 | |||||||
| chr12:112084045 | G | T | 1 | a0001c0001t0001g0180 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.403-2911C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084045 | |||||||
| chr12:112084401 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0255 |
2 | HG02683.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.403-3267G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084401 | |||||||
| chr12:112084542 | G | A | 77 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0020 others(74): Show |
77 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.402+3141C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084542 | |||||||
| chr12:112084661 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.402+3022C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084661 | |||||||
| chr12:112084779 | G | A | 4 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 others(1): Show |
4 | HG02280.hp1 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+2904C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084779 | |||||||
| chr12:112084881 | G | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.402+2802C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112084881 | |||||||
| chr12:112085014 | G | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.402+2669C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085014 | |||||||
| chr12:112085145 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.402+2538C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085145 | |||||||
| chr12:112085235 | C | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 others(2): Show |
5 | HG02622.hp1 HG02897.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+2448G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085235 | |||||||
| chr12:112085323 | CAG | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.402+2358_402+2359d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085323 | |||||||
| chr12:112085324 | A | G | 5 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+2359T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085324 | |||||||
| chr12:112085795 | G | A | 2 | a0002c0002t0002g0323 a0002c0002t0002g0324 |
2 | HG02135.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.402+1888C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085795 | |||||||
| chr12:112085874 | C | T | 33 | a0001c0001t0001g0122 a0003c0003t0001g0035 a0003c0003t0001g0036 others(30): Show |
33 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.402+1809G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112085874 | |||||||
| chr12:112086014 | CA | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0146 others(12): Show |
15 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.402+1668delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086014 | |||||||
| chr12:112086014 | CAA | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0113 others(25): Show |
28 | HG00099.hp1 HG00733.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.402+1667_402+1668d others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086014 | |||||||
| chr12:112086014 | CAAA | C | 8 | a0001c0001t0001g0152 a0001c0001t0001g0172 a0001c0001t0001g0174 others(5): Show |
8 | HG01256.hp2 HG02165.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+1666_402+1668d others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086014 | |||||||
| chr12:112086014 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.402+1654_402+1668d others(17): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086014 | |||||||
| chr12:112086014 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0173 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.402+1653_402+1668d others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086014 | |||||||
| chr12:112086035 | A | T | 1 | a0003c0003t0001g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.402+1648T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086035 | |||||||
| chr12:112086037 | A | T | 4 | a0001c0001t0001g0234 a0001c0001t0003g0055 a0003c0003t0001g0254 others(1): Show |
4 | HG00597.hp1 HG00733.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+1646T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086037 | |||||||
| chr12:112086039 | A | T | 11 | a0001c0001t0001g0234 a0001c0001t0003g0055 a0003c0003t0001g0119 others(8): Show |
11 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+1644T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086039 | |||||||
| chr12:112086041 | A | T | 13 | a0001c0001t0001g0234 a0001c0001t0003g0055 a0001c0001t0003g0085 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.402+1642T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086041 | |||||||
| chr12:112086043 | A | AT | 7 | a0001c0001t0003g0033 a0001c0001t0003g0074 a0003c0003t0001g0203 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+1639_402+1640i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086043 | |||||||
| chr12:112086043 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.402+1639_402+1640i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086043 | |||||||
| chr12:112086043 | A | T | 24 | a0001c0001t0001g0130 a0001c0001t0001g0181 a0001c0001t0001g0234 others(21): Show |
24 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.402+1640T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086043 | |||||||
| chr12:112086043 | AAAAAAAA others(3): Show |
A | 1 | a0003c0003t0001g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.402+1630_402+1639d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086043 | |||||||
| chr12:112086045 | A | AT | 7 | a0001c0001t0001g0144 a0001c0001t0003g0053 a0001c0001t0003g0095 others(4): Show |
7 | HG03453.hp2 HG03516.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+1637_402+1638i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086045 | |||||||
| chr12:112086045 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.402+1637_402+1638i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086045 | |||||||
| chr12:112086045 | A | T | 50 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0181 others(47): Show |
50 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.402+1638T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086045 | |||||||
| chr12:112086045 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.402+1628_402+1637d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086045 | |||||||
| chr12:112086047 | A | AT | 19 | a0001c0001t0003g0020 a0001c0001t0003g0025 a0001c0001t0003g0028 others(16): Show |
19 | HG01496.hp2 HG01891.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.402+1635_402+1636i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086047 | |||||||
| chr12:112086047 | A | ATATAT | 3 | a0001c0001t0001g0112 a0001c0001t0001g0140 a0001c0001t0001g0232 |
3 | NA18943.hp1 NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.402+1635_402+1636i others(7): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086047 | |||||||
| chr12:112086047 | A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0123 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | HG00140.hp2 HG01106.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1635_402+1636i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086047 | |||||||
| chr12:112086047 | A | T | 95 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0127 others(92): Show |
95 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.402+1636T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086047 | |||||||
| chr12:112086049 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0186 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.402+1633_402+1634i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086049 | |||||||
| chr12:112086049 | A | AT | 17 | a0001c0001t0001g0162 a0001c0001t0003g0042 a0001c0001t0003g0048 others(14): Show |
17 | HG01433.hp1 HG01496.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.402+1633_402+1634i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086049 | |||||||
| chr12:112086049 | A | ATAT | 4 | a0001c0001t0001g0131 a0001c0001t0001g0164 a0001c0001t0003g0100 others(1): Show |
4 | HG01993.hp1 HG02135.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+1633_402+1634i others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086049 | |||||||
| chr12:112086049 | A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0024 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.402+1633_402+1634i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086049 | |||||||
| chr12:112086049 | A | T | 206 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0118 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.402+1634T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086049 | |||||||
| chr12:112086051 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0003g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.402+1631_402+1632i others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0185 a0001c0001t0001g0188 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.402+1631_402+1632i others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0007g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.402+1631_402+1632i others(19): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | AAATATAT others(4): Show |
1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.402+1631_402+1632i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.402+1622_402+1631d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | AT | 7 | a0001c0001t0003g0049 a0001c0001t0003g0067 a0001c0001t0003g0213 others(4): Show |
7 | HG00597.hp2 HG02683.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1631_402+1632i others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | ATAT | 7 | a0001c0001t0003g0019 a0001c0001t0003g0040 a0001c0001t0003g0059 others(4): Show |
7 | HG01243.hp1 HG02132.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+1631_402+1632i others(5): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | ATATAT | 3 | a0001c0001t0003g0004 a0001c0001t0003g0093 a0002c0002t0002g0268 |
3 | HG02897.hp2 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.402+1631_402+1632i others(7): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.402+1631_402+1632i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086051 | A | T | 270 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.402+1632T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086051 | |||||||
| chr12:112086053 | T | A | 1 | a0001c0001t0007g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+1630A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086053 | |||||||
| chr12:112086063 | T | C | 1 | a0001c0001t0003g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.402+1620A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086063 | |||||||
| chr12:112086065 | T | C | 1 | a0001c0001t0003g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.402+1618A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086065 | |||||||
| chr12:112086067 | T | C | 5 | a0001c0001t0003g0055 a0001c0001t0003g0064 a0001c0001t0011g0253 others(2): Show |
5 | HG00597.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1616A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086067 | |||||||
| chr12:112086069 | T | C | 17 | a0001c0001t0003g0033 a0001c0001t0003g0054 a0001c0001t0003g0055 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.402+1614A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086069 | |||||||
| chr12:112086069 | TATATACA others(3): Show |
T | 2 | a0001c0001t0004g0108 a0001c0001t0004g0114 |
2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.402+1604_402+1613d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086069 | |||||||
| chr12:112086071 | T | C | 41 | a0001c0001t0001g0164 a0001c0001t0001g0252 a0001c0001t0003g0023 others(38): Show |
41 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.402+1612A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086071 | |||||||
| chr12:112086071 | T | TACACACA others(1): Show |
3 | a0003c0003t0001g0203 a0003c0003t0001g0206 a0003c0003t0001g0207 |
3 | HG01168.hp1 HG01169.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.402+1611_402+1612i others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086071 | |||||||
| chr12:112086071 | T | TACACACA others(3): Show |
1 | a0003c0003t0001g0208 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.402+1611_402+1612i others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086071 | |||||||
| chr12:112086071 | T | TACACACA others(11): Show |
1 | a0001c0001t0003g0049 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.402+1611_402+1612i others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086071 | |||||||
| chr12:112086073 | T | C | 112 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(109): Show |
114 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.402+1610A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TACAC | 12 | a0001c0001t0001g0011 a0001c0001t0001g0115 a0001c0001t0001g0123 others(9): Show |
12 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.402+1606_402+1609d others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TACACAC | 10 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0131 others(7): Show |
10 | HG01243.hp2 HG01993.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+1604_402+1609d others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0144 a0001c0001t0003g0029 a0001c0001t0003g0038 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+1600_402+1609d others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATACACA others(5): Show |
1 | a0002c0002t0002g0314 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATACACA others(7): Show |
1 | a0003c0003t0001g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATACACA others(9): Show |
3 | a0001c0001t0003g0058 a0001c0001t0003g0072 a0002c0002t0002g0291 |
3 | HG02071.hp1 HG02273.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATACACA others(11): Show |
4 | a0001c0001t0003g0092 a0002c0002t0002g0261 a0002c0002t0002g0266 others(1): Show |
4 | HG02056.hp2 NA18959.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+1609_402+1610i others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATACACA others(13): Show |
2 | a0001c0001t0003g0060 a0002c0002t0013g0319 |
2 | NA19057.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(3): Show |
1 | a0001c0001t0001g0135 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(5): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | NA19011.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(7): Show |
2 | a0003c0003t0001g0037 a0003c0003t0001g0089 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(11): Show |
1 | a0001c0001t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(13): Show |
1 | a0001c0001t0003g0101 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATACA others(17): Show |
2 | a0001c0001t0003g0050 a0001c0001t0003g0214 |
2 | HG03927.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(26): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(3): Show |
2 | a0003c0003t0001g0036 a0003c0003t0001g0246 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(5): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0181 a0001c0001t0001g0228 |
3 | HG03710.hp1 NA18949.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(7): Show |
1 | a0001c0001t0003g0039 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(9): Show |
2 | a0001c0001t0003g0082 a0003c0003t0001g0090 |
2 | HG02109.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(5): Show |
1 | a0003c0003t0001g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(7): Show |
5 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0142 others(2): Show |
5 | HG02602.hp1 HG02602.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+1609_402+1610i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(15): Show |
1 | a0001c0001t0015g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0134 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(9): Show |
3 | a0001c0001t0001g0128 a0001c0001t0001g0227 a0001c0001t0001g0249 |
3 | HG03492.hp2 HG03831.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.402+1609_402+1610i others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(15): Show |
1 | a0001c0001t0003g0002 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(19): Show |
1 | a0001c0001t0003g0025 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(15): Show |
1 | a0001c0001t0003g0028 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(17): Show |
1 | a0001c0001t0003g0026 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(26): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(15): Show |
1 | a0001c0001t0007g0235 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(17): Show |
1 | a0001c0001t0003g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(26): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(19): Show |
1 | a0001c0001t0007g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.402+1609_402+1610i others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(19): Show |
1 | a0001c0001t0007g0124 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0236 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | T | TATATATA others(23): Show |
1 | a0003c0003t0001g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.402+1609_402+1610i others(32): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086073 | TACACAC | T | 3 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0109 |
3 | HG01943.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.402+1604_402+1609d others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086073 | |||||||
| chr12:112086075 | C | T | 6 | a0001c0001t0001g0147 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
6 | HG01255.hp2 HG01361.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+1608G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086075 | |||||||
| chr12:112086077 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0244 others(1): Show |
4 | HG01361.hp1 HG01943.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.402+1606G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086077 | |||||||
| chr12:112086079 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0003g0111 a0006c0005t0017g0105 |
3 | HG01943.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.402+1604G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086079 | |||||||
| chr12:112086102 | A | ACACACAC others(6): Show |
1 | a0002c0002t0002g0298 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.402+1580_402+1581i others(15): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(8): Show |
1 | a0002c0002t0002g0309 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.402+1580_402+1581i others(17): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(19): Show |
1 | a0001c0001t0003g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.402+1580_402+1581i others(28): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(15): Show |
2 | a0001c0001t0003g0067 a0001c0001t0003g0084 |
2 | HG02738.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.402+1580_402+1581i others(24): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(13): Show |
6 | a0001c0001t0003g0034 a0001c0001t0003g0040 a0001c0001t0003g0041 others(3): Show |
6 | HG02132.hp1 HG02523.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(22): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(14): Show |
1 | a0001c0001t0003g0081 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.402+1580_402+1581i others(23): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(11): Show |
17 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0047 others(14): Show |
17 | HG01243.hp1 HG02129.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(20): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(9): Show |
19 | a0001c0001t0003g0052 a0001c0001t0003g0059 a0001c0001t0003g0093 others(16): Show |
19 | HG01496.hp2 HG02027.hp2 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(18): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(7): Show |
28 | a0001c0001t0003g0073 a0001c0001t0003g0095 a0001c0001t0003g0099 others(25): Show |
28 | HG00597.hp2 HG00735.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(16): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(5): Show |
21 | a0001c0001t0003g0004 a0001c0001t0003g0044 a0001c0001t0003g0045 others(18): Show |
21 | HG01081.hp1 HG01891.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(14): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(3): Show |
17 | a0001c0001t0003g0027 a0001c0001t0003g0032 a0001c0001t0003g0033 others(14): Show |
17 | HG01891.hp1 HG02109.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(12): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACAC others(1): Show |
8 | a0001c0001t0003g0031 a0001c0001t0003g0088 a0001c0001t0003g0216 others(5): Show |
8 | HG02717.hp2 HG02723.hp2 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACACC | 26 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(23): Show |
28 | HG00544.hp2 HG02132.hp2 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.402+1580_402+1581i others(8): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | ACACC | 3 | a0001c0001t0003g0055 a0002c0002t0002g0285 a0002c0002t0002g0333 |
3 | HG00597.hp1 NA18985.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.402+1580_402+1581i others(6): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086102 | A | C | 31 | a0001c0001t0001g0190 a0001c0001t0001g0212 a0001c0001t0003g0002 others(28): Show |
31 | HG01109.hp2 HG01123.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.402+1581T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086102 | |||||||
| chr12:112086103 | C | CACACACA others(4): Show |
1 | a0001c0001t0003g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.402+1579_402+1580i others(13): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086103 | |||||||
| chr12:112086104 | C | A | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.402+1579G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086104 | |||||||
| chr12:112086166 | C | T | 189 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(186): Show |
191 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(188): Show |
intron_variant | MODIFIER | c.402+1517G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086166 | |||||||
| chr12:112086491 | T | C | 1 | a0003c0003t0008g0102 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.402+1192A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086491 | |||||||
| chr12:112086622 | G | A | 15 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(12): Show |
15 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.402+1061C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086622 | |||||||
| chr12:112086713 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.402+970T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086713 | |||||||
| chr12:112086793 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.402+890G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086793 | |||||||
| chr12:112086823 | C | G | 1 | a0001c0001t0003g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.402+860G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086823 | |||||||
| chr12:112086829 | T | C | 1 | a0001c0001t0003g0218 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.402+854A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112086829 | |||||||
| chr12:112087009 | C | CA | 7 | a0001c0001t0001g0122 a0001c0001t0001g0178 a0001c0001t0001g0228 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+673dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112087009 | |||||||
| chr12:112087009 | CA | C | 180 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0020 others(177): Show |
182 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(179): Show |
intron_variant | MODIFIER | c.402+673delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112087009 | |||||||
| chr12:112087269 | C | T | 223 | a0001c0001t0001g0122 a0001c0001t0001g0212 a0001c0001t0003g0002 others(220): Show |
225 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(222): Show |
intron_variant | MODIFIER | c.402+414G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112087269 | |||||||
| chr12:112087605 | T | C | 1 | a0003c0003t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.402+78A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112087605 | |||||||
| chr12:112087618 | C | A | 1 | a0003c0003t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.402+65G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 4/23 | chr12 | 112087618 | |||||||
| chr12:112087892 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.284-91G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112087892 | |||||||
| chr12:112088317 | G | GT | 57 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0112 others(54): Show |
57 | HG00735.hp2 HG01106.hp1 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.284-517dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088317 | |||||||
| chr12:112088317 | G | GTT | 61 | a0001c0001t0001g0117 a0001c0001t0001g0127 a0001c0001t0001g0166 others(58): Show |
61 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.284-518_284-517dup others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088317 | |||||||
| chr12:112088317 | G | GTTT | 13 | a0001c0001t0001g0241 a0001c0001t0003g0033 a0001c0001t0003g0040 others(10): Show |
13 | HG01978.hp2 HG02027.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-519_284-517dup others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088317 | |||||||
| chr12:112088317 | GT | G | 84 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(81): Show |
86 | HG00544.hp2 HG00735.hp1 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.284-517delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088317 | |||||||
| chr12:112088360 | T | C | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-559A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088360 | |||||||
| chr12:112088365 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-564G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088365 | |||||||
| chr12:112088470 | C | T | 1 | a0001c0001t0003g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284-669G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088470 | |||||||
| chr12:112088531 | T | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.284-730A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088531 | |||||||
| chr12:112088623 | C | CT | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0170 others(3): Show |
6 | HG01255.hp1 HG01255.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-823dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088623 | |||||||
| chr12:112088623 | CT | C | 8 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0028 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-823delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088623 | |||||||
| chr12:112088911 | C | T | 1 | a0003c0003t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.284-1110G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112088911 | |||||||
| chr12:112089242 | T | C | 7 | a0001c0001t0003g0044 a0001c0001t0003g0072 a0001c0001t0003g0073 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-1441A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112089242 | |||||||
| chr12:112089336 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0239 |
2 | HG01175.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.283+1390A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112089336 | |||||||
| chr12:112089656 | T | G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.283+1070A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112089656 | |||||||
| chr12:112089977 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+749C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112089977 | |||||||
| chr12:112090178 | T | C | 1 | a0003c0003t0001g0254 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.283+548A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112090178 | |||||||
| chr12:112090661 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.283+65T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 3/23 | chr12 | 112090661 | |||||||
| chr12:112090999 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.145-135C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112090999 | |||||||
| chr12:112091011 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.145-147A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091011 | |||||||
| chr12:112091032 | C | G | 8 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.145-168G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091032 | |||||||
| chr12:112091244 | GA | G | 6 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0003c0003t0001g0221 others(3): Show |
6 | HG01891.hp2 HG03098.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.145-381delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091244 | |||||||
| chr12:112091250 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.145-386T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091250 | |||||||
| chr12:112091268 | T | C | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.145-404A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091268 | |||||||
| chr12:112091292 | C | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.145-428G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091292 | |||||||
| chr12:112091295 | A | T | 2 | a0003c0003t0001g0246 a0003c0003t0001g0247 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.145-431T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091295 | |||||||
| chr12:112091454 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.145-590G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091454 | |||||||
| chr12:112091519 | C | A | 2 | a0002c0002t0002g0326 a0002c0002t0002g0327 |
2 | HG02080.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.145-655G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091519 | |||||||
| chr12:112091617 | C | T | 2 | a0003c0003t0001g0246 a0003c0003t0001g0247 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.145-753G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091617 | |||||||
| chr12:112091711 | A | C | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.145-847T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091711 | |||||||
| chr12:112091999 | G | C | 6 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.144+1052C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112091999 | |||||||
| chr12:112092015 | C | T | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+1036G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092015 | |||||||
| chr12:112092240 | C | CA | 20 | a0001c0001t0003g0054 a0001c0001t0004g0114 a0002c0002t0002g0008 others(17): Show |
20 | HG02109.hp1 HG02135.hp2 HG02148.hp1 others(17): Show |
intron_variant | MODIFIER | c.144+810dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092240 | |||||||
| chr12:112092240 | C | CAA | 4 | a0002c0002t0002g0284 a0002c0002t0002g0299 a0002c0002t0002g0328 others(1): Show |
4 | HG02074.hp1 NA18950.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+809_144+810dup others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092240 | |||||||
| chr12:112092247 | G | A | 97 | a0001c0001t0003g0054 a0001c0001t0003g0111 a0001c0001t0004g0106 others(94): Show |
99 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.144+804C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092247 | |||||||
| chr12:112092247 | G | GA | 7 | a0001c0001t0001g0018 a0001c0001t0001g0187 a0001c0001t0001g0189 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+803dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092247 | |||||||
| chr12:112092284 | T | C | 1 | a0003c0003t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.144+767A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092284 | |||||||
| chr12:112092322 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.144+729C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092322 | |||||||
| chr12:112092622 | A | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0039 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.144+429T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092622 | |||||||
| chr12:112092656 | G | A | 1 | a0002c0002t0002g0300 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.144+395C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092656 | |||||||
| chr12:112092681 | C | A | 1 | a0001c0001t0014g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.144+370G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092681 | |||||||
| chr12:112092682 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.144+369G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092682 | |||||||
| chr12:112092682 | CT | C | 101 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(98): Show |
103 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.144+368delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092682 | |||||||
| chr12:112092683 | T | C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0003g0024 others(1): Show |
4 | HG03139.hp1 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+368A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092683 | |||||||
| chr12:112092869 | G | A | 3 | a0003c0003t0008g0102 a0003c0003t0008g0103 a0003c0003t0008g0104 |
3 | HG03098.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.144+182C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092869 | |||||||
| chr12:112092879 | T | C | 1 | a0003c0003t0008g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.144+172A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092879 | |||||||
| chr12:112092898 | A | G | 190 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(187): Show |
192 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(189): Show |
intron_variant | MODIFIER | c.144+153T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 2/23 | chr12 | 112092898 | |||||||
| chr12:112093273 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0135 others(1): Show |
4 | HG02135.hp1 NA18954.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-137G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112093273 | |||||||
| chr12:112093310 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.59-174G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112093310 | |||||||
| chr12:112093573 | A | G | 1 | a0003c0003t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.59-437T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112093573 | |||||||
| chr12:112093832 | C | T | 3 | a0001c0001t0003g0052 a0001c0001t0003g0055 a0001c0001t0003g0096 |
3 | HG00597.hp1 NA18965.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.59-696G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112093832 | |||||||
| chr12:112093909 | A | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.59-773T>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112093909 | |||||||
| chr12:112094134 | G | A | 5 | a0001c0001t0005g0077 a0001c0001t0005g0078 a0001c0001t0005g0079 others(2): Show |
5 | HG01167.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-998C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094134 | |||||||
| chr12:112094240 | C | CA | 95 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0135 others(92): Show |
97 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.59-1105dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094240 | |||||||
| chr12:112094240 | CA | C | 37 | a0001c0001t0001g0211 a0001c0001t0001g0249 a0001c0001t0003g0002 others(34): Show |
37 | HG01099.hp1 HG01167.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.59-1105delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094240 | |||||||
| chr12:112094240 | CAAAAAAA others(3): Show |
C | 50 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0003g0034 others(47): Show |
50 | HG00597.hp1 HG01243.hp1 HG02027.hp1 others(47): Show |
intron_variant | MODIFIER | c.59-1114_59-1105del others(10): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094240 | |||||||
| chr12:112094355 | T | A | 1 | a0002c0002t0002g0334 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.59-1219A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094355 | |||||||
| chr12:112094622 | A | G | 2 | a0003c0003t0008g0102 a0003c0003t0008g0104 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.59-1486T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112094622 | |||||||
| chr12:112095086 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-1950C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095086 | |||||||
| chr12:112095187 | C | T | 1 | a0003c0003t0008g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59-2051G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095187 | |||||||
| chr12:112095190 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.59-2054G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095190 | |||||||
| chr12:112095233 | T | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
4 | HG00140.hp2 HG00738.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-2097A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095233 | |||||||
| chr12:112095435 | T | TA | 98 | a0001c0001t0003g0054 a0001c0001t0003g0111 a0001c0001t0004g0106 others(95): Show |
100 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.59-2300dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095435 | |||||||
| chr12:112095524 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.59-2388C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095524 | |||||||
| chr12:112095619 | C | CA | 12 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0169 others(9): Show |
12 | HG01175.hp1 HG01175.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2484dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095619 | |||||||
| chr12:112095623 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.59-2487T>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095623 | |||||||
| chr12:112095636 | G | A | 1 | a0002c0002t0002g0267 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.59-2500C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095636 | |||||||
| chr12:112095958 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0227 |
3 | HG02602.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.59-2822G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095958 | |||||||
| chr12:112095970 | C | T | 19 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0262 others(16): Show |
21 | HG02132.hp2 NA18747.hp1 NA18939.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-2834G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112095970 | |||||||
| chr12:112096060 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0082 |
2 | HG02074.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.59-2924C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096060 | |||||||
| chr12:112096063 | G | A | 1 | a0003c0003t0001g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.59-2927C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096063 | |||||||
| chr12:112096126 | C | T | 1 | a0001c0001t0014g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.59-2990G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096126 | |||||||
| chr12:112096203 | A | G | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.59-3067T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096203 | |||||||
| chr12:112096228 | A | G | 3 | a0002c0002t0002g0269 a0002c0002t0002g0270 a0002c0002t0002g0271 |
3 | NA18948.hp2 NA18964.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.59-3092T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096228 | |||||||
| chr12:112096325 | A | G | 1 | a0006c0005t0017g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.59-3189T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096325 | |||||||
| chr12:112096855 | C | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-3719G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096855 | |||||||
| chr12:112096975 | T | C | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59-3839A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112096975 | |||||||
| chr12:112097098 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.59-3962G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097098 | |||||||
| chr12:112097326 | G | A | 1 | a0002c0002t0002g0333 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.59-4190C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097326 | |||||||
| chr12:112097381 | G | A | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.59-4245C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097381 | |||||||
| chr12:112097479 | C | T | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4343G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097479 | |||||||
| chr12:112097562 | G | T | 4 | a0001c0001t0007g0124 a0001c0001t0007g0125 a0001c0001t0007g0126 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-4426C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097562 | |||||||
| chr12:112097606 | C | CA | 29 | a0001c0001t0001g0012 a0001c0001t0001g0144 a0001c0001t0001g0178 others(26): Show |
29 | HG00735.hp1 HG01071.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-4471dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097606 | |||||||
| chr12:112097606 | CA | C | 10 | a0001c0001t0001g0189 a0001c0001t0003g0111 a0001c0001t0004g0106 others(7): Show |
10 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-4471delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097606 | |||||||
| chr12:112097654 | A | G | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-4518T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097654 | |||||||
| chr12:112097655 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.59-4519C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097655 | |||||||
| chr12:112097989 | C | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4853G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112097989 | |||||||
| chr12:112098043 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.59-4907G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098043 | |||||||
| chr12:112098085 | C | T | 1 | a0002c0002t0002g0335 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.59-4949G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098085 | |||||||
| chr12:112098119 | C | CA | 195 | a0001c0001t0001g0018 a0001c0001t0001g0112 a0001c0001t0001g0117 others(192): Show |
197 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.59-4984dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098119 | |||||||
| chr12:112098119 | C | CAA | 35 | a0001c0001t0001g0115 a0001c0001t0001g0140 a0001c0001t0001g0141 others(32): Show |
35 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.59-4985_59-4984dup others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098119 | |||||||
| chr12:112098119 | C | CAAA | 31 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(28): Show |
31 | HG00099.hp2 HG00733.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-4986_59-4984dup others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098119 | |||||||
| chr12:112098119 | C | CAAAA | 6 | a0003c0003t0001g0090 a0003c0003t0001g0145 a0003c0003t0001g0210 others(3): Show |
6 | HG01175.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-4987_59-4984dup others(4): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098119 | |||||||
| chr12:112098119 | CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-4994_59-4984del others(11): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098119 | |||||||
| chr12:112098325 | C | T | 2 | a0002c0002t0009g0258 a0002c0002t0009g0332 |
2 | NA18981.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.59-5189G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098325 | |||||||
| chr12:112098451 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-5315A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112098451 | |||||||
| chr12:112099287 | C | CT | 215 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0001t0001g0186 others(212): Show |
217 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.59-6152dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099287 | |||||||
| chr12:112099287 | C | CTT | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(9): Show |
12 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-6153_59-6152dup others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099287 | |||||||
| chr12:112099500 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.59-6364G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099500 | |||||||
| chr12:112099557 | T | C | 6 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0007 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-6421A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099557 | |||||||
| chr12:112099682 | C | G | 16 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(13): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-6546G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099682 | |||||||
| chr12:112099715 | T | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.59-6579A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099715 | |||||||
| chr12:112099764 | A | G | 16 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(13): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-6628T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099764 | |||||||
| chr12:112099827 | T | A | 1 | a0001c0001t0003g0038 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.59-6691A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099827 | |||||||
| chr12:112099901 | T | A | 2 | a0002c0002t0002g0266 a0002c0002t0013g0319 |
2 | NA19057.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.59-6765A>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099901 | |||||||
| chr12:112099934 | T | C | 80 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(77): Show |
80 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.59-6798A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099934 | |||||||
| chr12:112099940 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.59-6804G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112099940 | |||||||
| chr12:112100053 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.59-6917A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100053 | |||||||
| chr12:112100160 | ACATTTGC others(62): Show |
A | 1 | a0001c0001t0001g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.59-7093_59-7025del others(69): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100160 | |||||||
| chr12:112100383 | G | C | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.59-7247C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100383 | |||||||
| chr12:112100458 | G | C | 2 | a0001c0001t0003g0019 a0004c0008t0003g0021 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.59-7322C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100458 | |||||||
| chr12:112100524 | G | A | 1 | a0001c0001t0004g0109 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.59-7388C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100524 | |||||||
| chr12:112100614 | C | CT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0146 others(20): Show |
23 | HG00140.hp1 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-7479dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100614 | |||||||
| chr12:112100614 | C | CTT | 76 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(73): Show |
78 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.59-7480_59-7479dup others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100614 | |||||||
| chr12:112100614 | C | CTTT | 8 | a0002c0002t0002g0257 a0002c0002t0002g0262 a0002c0002t0002g0263 others(5): Show |
8 | HG01952.hp2 HG02080.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-7481_59-7479dup others(3): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100614 | |||||||
| chr12:112100614 | CT | C | 18 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0202 others(15): Show |
18 | HG01071.hp2 HG01256.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-7479delA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100614 | |||||||
| chr12:112100654 | C | G | 1 | a0001c0001t0003g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.59-7518G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100654 | |||||||
| chr12:112100693 | C | T | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-7557G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100693 | |||||||
| chr12:112100870 | G | T | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-7734C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100870 | |||||||
| chr12:112100909 | C | T | 74 | a0001c0001t0003g0020 a0001c0001t0003g0033 a0001c0001t0003g0034 others(71): Show |
74 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.59-7773G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112100909 | |||||||
| chr12:112101059 | G | C | 3 | a0002c0002t0002g0323 a0002c0002t0002g0324 a0002c0002t0002g0325 |
3 | HG02027.hp2 HG02135.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.58+7657C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101059 | |||||||
| chr12:112101188 | T | C | 8 | a0001c0001t0003g0111 a0001c0001t0004g0106 a0001c0001t0004g0107 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+7528A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101188 | |||||||
| chr12:112101244 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.58+7472A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101244 | |||||||
| chr12:112101372 | C | T | 3 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 |
3 | NA18971.hp2 NA18980.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.58+7344G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101372 | |||||||
| chr12:112101475 | GGCCGGGT others(12): Show |
G | 2 | a0002c0002t0002g0326 a0002c0002t0002g0327 |
2 | HG02080.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.58+7222_58+7240del others(19): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101475 | |||||||
| chr12:112101675 | T | C | 1 | a0003c0003t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58+7041A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101675 | |||||||
| chr12:112101712 | A | G | 268 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(265): Show |
270 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(267): Show |
intron_variant | MODIFIER | c.58+7004T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101712 | |||||||
| chr12:112101729 | C | T | 1 | a0002c0002t0002g0261 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.58+6987G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101729 | |||||||
| chr12:112101868 | C | CT | 8 | a0001c0001t0001g0251 a0001c0001t0003g0111 a0001c0001t0004g0106 others(5): Show |
8 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+6847dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112101868 | |||||||
| chr12:112102305 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.58+6411G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102305 | |||||||
| chr12:112102305 | C | T | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+6411G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102305 | |||||||
| chr12:112102319 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.58+6397C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102319 | |||||||
| chr12:112102698 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58+6018C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102698 | |||||||
| chr12:112102713 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.58+6003C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102713 | |||||||
| chr12:112102773 | G | A | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.58+5943C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102773 | |||||||
| chr12:112102854 | T | C | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+5862A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102854 | |||||||
| chr12:112102894 | C | T | 1 | a0003c0003t0008g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58+5822G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112102894 | |||||||
| chr12:112103073 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.58+5643C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112103073 | |||||||
| chr12:112103123 | G | T | 1 | a0001c0001t0003g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58+5593C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112103123 | |||||||
| chr12:112103131 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+5585G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112103131 | |||||||
| chr12:112104089 | G | T | 1 | a0003c0003t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.58+4627C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104089 | |||||||
| chr12:112104179 | G | A | 93 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0019 others(90): Show |
93 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(90): Show |
intron_variant | MODIFIER | c.58+4537C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104179 | |||||||
| chr12:112104416 | G | T | 4 | a0003c0003t0001g0221 a0003c0003t0008g0102 a0003c0003t0008g0103 others(1): Show |
4 | HG03098.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+4300C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104416 | |||||||
| chr12:112104576 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.58+4140G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104576 | |||||||
| chr12:112104697 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0242 |
3 | HG01109.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.58+4019C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104697 | |||||||
| chr12:112104709 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4007C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104709 | |||||||
| chr12:112104835 | C | CA | 97 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(94): Show |
97 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.58+3880dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104835 | |||||||
| chr12:112104847 | C | A | 88 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(85): Show |
90 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.58+3869G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104847 | |||||||
| chr12:112104959 | G | C | 1 | a0002c0002t0002g0331 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.58+3757C>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112104959 | |||||||
| chr12:112105196 | T | G | 9 | a0003c0003t0001g0203 a0003c0003t0001g0204 a0003c0003t0001g0205 others(6): Show |
9 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3520A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112105196 | |||||||
| chr12:112105377 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.58+3339G>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112105377 | |||||||
| chr12:112105860 | C | G | 7 | a0001c0001t0004g0106 a0001c0001t0004g0107 a0001c0001t0004g0108 others(4): Show |
7 | HG01943.hp1 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+2856G>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112105860 | |||||||
| chr12:112105873 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.58+2843A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112105873 | |||||||
| chr12:112106077 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.58+2639G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106077 | |||||||
| chr12:112106094 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0249 |
2 | NA19004.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.58+2622A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106094 | |||||||
| chr12:112106391 | T | TA | 73 | a0001c0001t0001g0212 a0001c0001t0003g0002 a0001c0001t0003g0004 others(70): Show |
73 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+2324dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106391 | |||||||
| chr12:112106821 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.58+1895G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106821 | |||||||
| chr12:112106955 | C | CA | 46 | a0001c0001t0001g0018 a0001c0001t0001g0227 a0001c0001t0001g0228 others(43): Show |
46 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+1760dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106955 | |||||||
| chr12:112106955 | CA | C | 25 | a0001c0001t0001g0112 a0001c0001t0003g0023 a0001c0001t0003g0024 others(22): Show |
25 | HG01943.hp1 HG02257.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.58+1760delT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106955 | |||||||
| chr12:112106955 | CAA | C | 82 | a0001c0001t0011g0253 a0002c0002t0002g0001 a0002c0002t0002g0005 others(79): Show |
84 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.58+1759_58+1760del others(2): Show |
NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112106955 | |||||||
| chr12:112107227 | T | C | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.58+1489A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107227 | |||||||
| chr12:112107381 | G | GT | 6 | a0001c0001t0003g0019 a0003c0003t0008g0102 a0003c0003t0008g0103 others(3): Show |
6 | HG01891.hp1 HG02559.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+1334dupA | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107381 | |||||||
| chr12:112107393 | G | T | 89 | a0001c0001t0001g0011 a0001c0001t0003g0002 a0001c0001t0003g0004 others(86): Show |
89 | HG00597.hp1 HG01081.hp1 HG01099.hp1 others(86): Show |
intron_variant | MODIFIER | c.58+1323C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107393 | |||||||
| chr12:112107396 | G | T | 4 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1320C>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107396 | |||||||
| chr12:112107569 | T | TA | 90 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0002c0002t0002g0001 others(87): Show |
92 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.58+1146dupT | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107569 | |||||||
| chr12:112107570 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG00738.hp2 HG01928.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+1146T>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107570 | |||||||
| chr12:112107931 | G | A | 1 | a0001c0001t0011g0253 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.58+785C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107931 | |||||||
| chr12:112107940 | T | C | 1 | a0003c0003t0001g0254 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.58+776A>G | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112107940 | |||||||
| chr12:112108031 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58+685A>C | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108031 | |||||||
| chr12:112108179 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.58+537G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108179 | |||||||
| chr12:112108181 | G | A | 1 | a0003c0003t0001g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+535C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108181 | |||||||
| chr12:112108379 | C | T | 89 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(86): Show |
91 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.58+337G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108379 | |||||||
| chr12:112108541 | G | A | 83 | a0002c0002t0002g0001 a0002c0002t0002g0257 a0002c0002t0002g0259 others(80): Show |
85 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.58+175C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108541 | |||||||
| chr12:112108549 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.58+167C>T | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108549 | |||||||
| chr12:112108602 | C | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0015g0003 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.58+114G>A | NAA25 | ENSG00000111300.10 | transcript | ENST00000261745.9 | protein_coding | 1/23 | chr12 | 112108602 |