Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4908 |
| ensemblid | ENSG00000185652.12 |
| hgncid | 8023 |
| symbol | NTF3 |
| name | neurotrophin 3 |
| refseq_nuc | NM_001102654.2 |
| refseq_prot | NP_001096124.1 |
| ensembl_nuc | ENST00000423158.4 |
| ensembl_prot | ENSP00000397297.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 5432108 |
| end | 5495299 |
| strand | + |
| ver | v1.2 |
| region | chr12:5432108-5495299 |
| region5000 | chr12:5427108-5500299 |
| regionname0 | NTF3_chr12_5432108_5495299 |
| regionname5000 | NTF3_chr12_5427108_5500299 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 270 | 315 | 74 | 66 | 123 | 16 | 34 | 93 | NTF3_chr12_5427108_5500299 | NTF3 | MVTFA others(265): Show |
chr12 | 5427108 | 5500299 |
| a0002 | 0/0 | 270 | 54 | 17 | 10 | 25 | 0 | 2 | 21 | NTF3_chr12_5427108_5500299 | NTF3 | MVTFA others(265): Show |
chr12 | 5427108 | 5500299 |
| a0003 | 0/0 | 270 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | MVTFA others(265): Show |
chr12 | 5427108 | 5500299 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 810 | 155 | 52 | 32 | 57 | 5 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0002 | 1/0 | 810 | 132 | 17 | 27 | 60 | 10 | 17 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0004 | 0/0 | 810 | 21 | 4 | 5 | 3 | 1 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0006 | 0/0 | 810 | 3 | 0 | 2 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0007 | 0/0 | 810 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0009 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0001c0011 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0002c0003 | 0/0 | 810 | 49 | 17 | 10 | 21 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0002c0005 | 0/0 | 810 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0002c0010 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 | ||
| a0003c0008 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ATGGT others(805): Show |
chr12 | 5427108 | 5500299 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1341 | 151 | 49 | 31 | 57 | 5 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0001t0002 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0001t0003 | 0/0 | 1341 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0001t0004 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0001t0005 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0002t0001 | 1/0 | 1341 | 132 | 17 | 27 | 60 | 10 | 17 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0004t0001 | 0/0 | 1341 | 21 | 4 | 5 | 3 | 1 | 8 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0006t0001 | 0/0 | 1341 | 3 | 0 | 2 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0007t0001 | 0/0 | 1341 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0009t0001 | 0/0 | 1341 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0001c0011t0001 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0002c0003t0001 | 0/0 | 1341 | 49 | 17 | 10 | 21 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0002c0005t0001 | 0/0 | 1341 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0002c0010t0001 | 0/0 | 1341 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| a0003c0008t0001 | 0/0 | 1341 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | ACTCA others(1336): Show |
chr12 | 5427108 | 5500299 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0297 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0004t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0006t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0007t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0009t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0001c0011t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0003t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0005t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0005t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0005t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0002c0010t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| a0003c0008t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0163 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0347 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | GBR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0153 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | FIN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0330 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0054 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0285 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00673 | hp2 | a0001 | c0009 | t0001 | g0281 | EAS | CHS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0017 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01070 | hp1 | a0001 | c0004 | t0001 | g0017 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0284 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0136 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0010 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01169 | hp2 | a0001 | c0006 | t0001 | g0010 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0248 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0132 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0273 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01361 | hp1 | a0002 | c0003 | t0001 | g0083 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0090 | AMR | CLM | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0171 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0291 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0270 | EUR | IBS | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0165 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0317 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0305 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0128 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0129 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01975 | hp1 | a0002 | c0003 | t0001 | g0263 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0335 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0346 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0244 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | CDX | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0062 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0205 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0058 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0345 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02698 | hp2 | a0001 | c0006 | t0001 | g0092 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0188 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02723 | hp1 | a0001 | c0011 | t0001 | g0287 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0169 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0247 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0271 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0072 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0107 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0139 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03017 | hp2 | a0001 | c0004 | t0001 | g0312 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0207 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0343 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0059 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0160 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0057 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0147 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0342 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0290 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0111 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03704 | hp2 | a0002 | c0010 | t0001 | g0316 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0251 | SAS | PJL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0150 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0170 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0250 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0069 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0155 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0315 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | CHB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18906 | hp1 | a0003 | c0008 | t0001 | g0045 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18952 | hp1 | a0002 | c0005 | t0001 | g0257 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18959 | hp1 | a0002 | c0005 | t0001 | g0308 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0301 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18970 | hp2 | a0002 | c0005 | t0001 | g0255 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0005 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18974 | hp1 | a0002 | c0003 | t0001 | g0314 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18977 | hp1 | a0001 | c0007 | t0001 | g0211 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18985 | hp1 | a0002 | c0003 | t0001 | g0015 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18991 | hp1 | a0001 | c0007 | t0001 | g0066 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18991 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19004 | hp2 | a0001 | c0004 | t0001 | g0267 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19010 | hp2 | a0002 | c0005 | t0001 | g0256 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0229 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ASW | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0197 | AFR | ASW | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0095 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0230 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0241 | SAS | GIH | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0286 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0208 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | USA | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0297 | REF | REF | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0027 | REF | REF | NTF3_chr12_5427108_5500299 | NTF3 | chr12 | 5427108 | 5500299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:5494440 | G | A | 1 | a0002 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.265G>A | p.Gly89Arg | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 482/1341 | 265/813 | 89/270 | chr12 | 5494440 | |||
| chr12:5494441 | G | A | 2 | a0002 a0003 |
54 | HG00408.hp1 HG00408.hp2 HG01106.hp1 others(51): Show |
missense_variant | MODERATE | c.266G>A | p.Gly89Glu | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 483/1341 | 266/813 | 89/270 | chr12 | 5494441 | |||
| chr12:5494563 | T | G | 1 | a0003 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.388T>G | p.Leu130Val | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 605/1341 | 388/813 | 130/270 | chr12 | 5494563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:5494436 | G | C | 4 | a0001c0009 a0002c0003 a0002c0005 others(1): Show |
55 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(52): Show |
synonymous_variant | LOW | c.261G>C | p.Arg87Arg | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 478/1341 | 261/813 | 87/270 | chr12 | 5494436 | |||
| chr12:5494466 | G | A | 3 | a0001c0001 a0001c0004 a0001c0011 |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
synonymous_variant | LOW | c.291G>A | p.Pro97Pro | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 508/1341 | 291/813 | 97/270 | chr12 | 5494466 | |||
| chr12:5494769 | C | T | 3 | a0001c0004 a0001c0006 a0002c0005 |
28 | HG00738.hp1 HG01070.hp1 HG01168.hp1 others(25): Show |
synonymous_variant | LOW | c.594C>T | p.Pro198Pro | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 811/1341 | 594/813 | 198/270 | chr12 | 5494769 | |||
| chr12:5494823 | C | T | 1 | a0001c0007 | 2 | NA18977.hp1 NA18991.hp1 |
synonymous_variant | LOW | c.648C>T | p.Asn216Asn | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 865/1341 | 648/813 | 216/270 | chr12 | 5494823 | |||
| chr12:5494901 | A | G | 1 | a0001c0011 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.726A>G | p.Ser242Ser | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 943/1341 | 726/813 | 242/270 | chr12 | 5494901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:5432293 | T | C | 1 | a0001c0001t0002 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/2 | 32 | chr12 | 5432293 | ||||||
| chr12:5495031 | A | G | 1 | a0001c0001t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 43 | chr12 | 5495031 | ||||||
| chr12:5495234 | C | G | 1 | a0001c0001t0004 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 246 | chr12 | 5495234 | ||||||
| chr12:5495254 | T | G | 1 | a0001c0001t0003 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 2/2 | 266 | chr12 | 5495254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:5432439 | A | T | 1 | a0001c0002t0001g0347 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.18+97A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432439 | |||||||
| chr12:5432458 | C | G | 1 | a0001c0004t0001g0346 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.18+116C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432458 | |||||||
| chr12:5432540 | A | T | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+198A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432540 | |||||||
| chr12:5432541 | C | T | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+199C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432541 | |||||||
| chr12:5432556 | T | TAC | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG02647.hp1 HG02922.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+264_18+265dupCA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TAC | T | 14 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0056 others(11): Show |
14 | HG00408.hp2 HG01993.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+264_18+265delCA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACAC | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0061 others(68): Show |
76 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.18+262_18+265delCA others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACAC | T | 56 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(53): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+260_18+265delCA others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACACA others(1): Show |
T | 131 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
138 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.18+258_18+265delCA others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACACA others(3): Show |
T | 32 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0294 others(29): Show |
37 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.18+256_18+265delCA others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACACA others(5): Show |
T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0324 others(15): Show |
20 | HG00140.hp2 HG00408.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.18+254_18+265delCA others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+252_18+265delCA others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432556 | TACACACA others(11): Show |
T | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+248_18+265delCA others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432556 | ||||||
| chr12:5432580 | C | A | 1 | a0001c0002t0001g0022 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.18+238C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432580 | |||||||
| chr12:5432602 | C | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0056 a0001c0002t0001g0039 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+260C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432602 | |||||||
| chr12:5432650 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+308G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432650 | |||||||
| chr12:5432725 | A | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.18+383A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432725 | |||||||
| chr12:5432726 | A | C | 150 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.18+384A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432726 | |||||||
| chr12:5432868 | G | GC | 3 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0112 |
3 | HG02257.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+527dupC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5432868 | ||||||
| chr12:5432973 | G | T | 1 | a0001c0004t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+631G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5432973 | |||||||
| chr12:5433024 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.18+682G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433024 | |||||||
| chr12:5433141 | C | G | 65 | a0001c0001t0001g0019 a0001c0001t0001g0113 a0001c0001t0001g0115 others(62): Show |
66 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.18+799C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433141 | |||||||
| chr12:5433173 | TC | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG01891.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.18+833delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433173 | ||||||
| chr12:5433199 | C | T | 24 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0292 others(21): Show |
25 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433199 | |||||||
| chr12:5433368 | T | C | 66 | a0001c0001t0001g0019 a0001c0001t0001g0113 a0001c0001t0001g0115 others(63): Show |
67 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.18+1026T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433368 | |||||||
| chr12:5433448 | G | GGAGGGGC | 31 | a0001c0001t0001g0019 a0001c0001t0001g0168 a0001c0001t0001g0172 others(28): Show |
32 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.18+1112_18+1118dup others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433448 | ||||||
| chr12:5433454 | G | GCGAGGGC | 38 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0115 others(35): Show |
38 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+1120_18+1126dup others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433454 | ||||||
| chr12:5433521 | C | T | 1 | a0001c0002t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.18+1179C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433521 | |||||||
| chr12:5433597 | CTGAGACC others(2): Show |
C | 17 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0117 others(14): Show |
17 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+1258_18+1266del others(9): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5433597 | ||||||
| chr12:5433684 | G | T | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+1342G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433684 | |||||||
| chr12:5433704 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18+1362C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433704 | |||||||
| chr12:5433906 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.18+1564G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433906 | |||||||
| chr12:5433979 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.18+1637C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5433979 | |||||||
| chr12:5434074 | T | C | 2 | a0001c0002t0001g0022 a0001c0002t0001g0278 |
2 | HG00558.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.18+1732T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434074 | |||||||
| chr12:5434270 | G | T | 1 | a0001c0002t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+1928G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434270 | |||||||
| chr12:5434440 | G | A | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+2098G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434440 | |||||||
| chr12:5434472 | A | AGT | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0024 others(54): Show |
60 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.18+2163_18+2164dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGT | 25 | a0001c0001t0001g0222 a0001c0001t0001g0280 a0001c0001t0002g0338 others(22): Show |
25 | HG00558.hp1 HG00673.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+2161_18+2164dup others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGT | 37 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0056 others(34): Show |
41 | HG00438.hp1 HG00621.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.18+2159_18+2164dup others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGTG others(1): Show |
27 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0038 others(24): Show |
27 | HG00099.hp1 HG00738.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+2157_18+2164dup others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGTG others(3): Show |
6 | a0001c0001t0001g0167 a0001c0001t0001g0289 a0001c0001t0001g0320 others(3): Show |
6 | HG02970.hp2 HG03453.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+2155_18+2164dup others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0002t0001g0042 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+2153_18+2164dup others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0043 a0001c0002t0001g0230 a0001c0002t0001g0322 |
3 | HG02083.hp1 HG02809.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.18+2151_18+2164dup others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0172 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.18+2149_18+2164dup others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434472 | AGTGTGTG others(5): Show |
A | 1 | a0002c0003t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.18+2153_18+2164del others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5434472 | ||||||
| chr12:5434603 | A | G | 1 | a0001c0002t0001g0333 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.18+2261A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5434603 | |||||||
| chr12:5435017 | C | A | 1 | a0001c0002t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.18+2675C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435017 | |||||||
| chr12:5435031 | A | G | 1 | a0001c0001t0003g0033 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.18+2689A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435031 | |||||||
| chr12:5435067 | A | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0341 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+2725A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435067 | |||||||
| chr12:5435165 | T | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(33): Show |
37 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+2823T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435165 | |||||||
| chr12:5435459 | G | A | 31 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(28): Show |
32 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.18+3117G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435459 | |||||||
| chr12:5435559 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+3217A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435559 | |||||||
| chr12:5435739 | A | G | 5 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(2): Show |
5 | HG02622.hp2 HG03098.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+3397A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435739 | |||||||
| chr12:5435788 | G | A | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+3446G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435788 | |||||||
| chr12:5435828 | A | G | 297 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(294): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.18+3486A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435828 | |||||||
| chr12:5435832 | A | G | 38 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0158 others(35): Show |
39 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.18+3490A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435832 | |||||||
| chr12:5435853 | C | G | 1 | a0002c0010t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+3511C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435853 | |||||||
| chr12:5435889 | C | T | 1 | a0001c0002t0001g0014 | 2 | NA18955.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.18+3547C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5435889 | |||||||
| chr12:5436025 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.18+3683G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436025 | |||||||
| chr12:5436074 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+3732C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436074 | |||||||
| chr12:5436082 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0337 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+3740G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436082 | |||||||
| chr12:5436093 | C | T | 3 | a0001c0001t0001g0209 a0002c0003t0001g0207 a0002c0003t0001g0208 |
3 | HG02965.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.18+3751C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436093 | |||||||
| chr12:5436142 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18+3800T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436142 | |||||||
| chr12:5436225 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+3883T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436225 | |||||||
| chr12:5436326 | T | C | 1 | a0001c0002t0001g0323 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.18+3984T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436326 | |||||||
| chr12:5436334 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.18+3992A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436334 | |||||||
| chr12:5436366 | A | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(33): Show |
37 | HG00438.hp1 HG00621.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+4024A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436366 | |||||||
| chr12:5436809 | G | T | 1 | a0001c0002t0001g0268 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.18+4467G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436809 | |||||||
| chr12:5436818 | T | A | 1 | a0001c0007t0001g0066 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18+4476T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436818 | |||||||
| chr12:5436886 | A | G | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.18+4544A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436886 | |||||||
| chr12:5436924 | A | C | 5 | a0001c0002t0001g0046 a0001c0002t0001g0309 a0001c0002t0001g0311 others(2): Show |
5 | NA18957.hp1 NA18959.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+4582A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436924 | |||||||
| chr12:5436955 | G | T | 6 | a0001c0001t0001g0288 a0001c0001t0001g0302 a0001c0001t0001g0339 others(3): Show |
6 | HG01952.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+4613G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5436955 | |||||||
| chr12:5437157 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.18+4815C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437157 | |||||||
| chr12:5437158 | C | T | 1 | a0001c0002t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+4816C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437158 | |||||||
| chr12:5437300 | C | T | 2 | a0001c0001t0001g0204 a0001c0004t0001g0205 |
2 | HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.18+4958C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437300 | |||||||
| chr12:5437322 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.18+4980A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437322 | |||||||
| chr12:5437390 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.18+5048A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437390 | |||||||
| chr12:5437404 | G | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0146 others(39): Show |
46 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.18+5062G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437404 | |||||||
| chr12:5437476 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0037 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.18+5134G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437476 | |||||||
| chr12:5437668 | G | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0065 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+5326G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437668 | |||||||
| chr12:5437687 | G | T | 12 | a0001c0001t0001g0158 a0001c0001t0001g0280 a0001c0002t0001g0022 others(9): Show |
12 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+5345G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437687 | |||||||
| chr12:5437745 | A | T | 32 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(29): Show |
33 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.18+5403A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437745 | |||||||
| chr12:5437798 | G | A | 1 | a0001c0006t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.18+5456G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437798 | |||||||
| chr12:5437930 | T | C | 32 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(29): Show |
33 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.18+5588T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437930 | |||||||
| chr12:5437978 | T | G | 2 | a0001c0001t0001g0302 a0001c0001t0001g0341 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+5636T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5437978 | |||||||
| chr12:5438021 | A | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0044 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+5679A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438021 | |||||||
| chr12:5438067 | A | C | 3 | a0001c0001t0001g0109 a0001c0002t0001g0008 a0001c0002t0001g0221 |
4 | HG01074.hp2 HG01516.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+5725A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438067 | |||||||
| chr12:5438227 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+5885C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438227 | |||||||
| chr12:5438559 | AT | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0172 others(23): Show |
27 | HG00438.hp1 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+6226delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5438559 | ||||||
| chr12:5438593 | G | T | 40 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0037 others(37): Show |
41 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.18+6251G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438593 | |||||||
| chr12:5438702 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG02647.hp1 HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.18+6360G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438702 | |||||||
| chr12:5438705 | G | A | 1 | a0001c0002t0001g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.18+6363G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438705 | |||||||
| chr12:5438789 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0341 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+6447G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438789 | |||||||
| chr12:5438998 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0337 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+6656G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5438998 | |||||||
| chr12:5439005 | A | T | 17 | a0001c0001t0001g0158 a0001c0001t0001g0280 a0001c0002t0001g0022 others(14): Show |
17 | HG00558.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+6663A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439005 | |||||||
| chr12:5439131 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+6789T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439131 | |||||||
| chr12:5439135 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(244): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.18+6793C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439135 | |||||||
| chr12:5439254 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+6912C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439254 | |||||||
| chr12:5439275 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0252 a0001c0002t0001g0234 others(1): Show |
4 | HG00642.hp2 HG00735.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+6933T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439275 | |||||||
| chr12:5439495 | T | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(56): Show |
67 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+7153T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439495 | |||||||
| chr12:5439502 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0043 others(5): Show |
8 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+7160G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439502 | |||||||
| chr12:5439518 | T | A | 1 | a0001c0002t0001g0067 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.18+7176T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439518 | |||||||
| chr12:5439649 | G | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+7307G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439649 | |||||||
| chr12:5439688 | A | G | 1 | a0001c0002t0001g0185 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.18+7346A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439688 | |||||||
| chr12:5439751 | A | G | 1 | a0001c0004t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+7409A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5439751 | |||||||
| chr12:5440037 | A | G | 34 | a0001c0001t0001g0019 a0001c0001t0001g0146 a0001c0001t0001g0168 others(31): Show |
35 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.18+7695A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440037 | |||||||
| chr12:5440106 | C | G | 1 | a0001c0002t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.18+7764C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440106 | |||||||
| chr12:5440290 | C | T | 37 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0037 others(34): Show |
38 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+7948C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440290 | |||||||
| chr12:5440330 | T | C | 6 | a0001c0001t0001g0288 a0001c0001t0001g0302 a0001c0001t0001g0339 others(3): Show |
6 | HG01952.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+7988T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440330 | |||||||
| chr12:5440406 | C | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(33): Show |
37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8064C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440406 | |||||||
| chr12:5440466 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0341 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+8124G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440466 | |||||||
| chr12:5440550 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0236 a0001c0004t0001g0251 |
3 | HG00735.hp1 HG01069.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.18+8208G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440550 | |||||||
| chr12:5440697 | A | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(33): Show |
37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8355A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5440697 | |||||||
| chr12:5441172 | T | C | 36 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(33): Show |
37 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+8830T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441172 | |||||||
| chr12:5441376 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG01952.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+9034C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441376 | |||||||
| chr12:5441468 | AT | A | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9128delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5441468 | ||||||
| chr12:5441471 | G | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9129G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441471 | |||||||
| chr12:5441475 | A | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9133A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441475 | |||||||
| chr12:5441477 | CCTGGG | C | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9136_18+9140del others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441477 | |||||||
| chr12:5441572 | G | A | 35 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0146 others(32): Show |
36 | HG00438.hp1 HG00738.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.18+9230G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441572 | |||||||
| chr12:5441652 | G | A | 2 | a0001c0001t0001g0288 a0001c0002t0001g0156 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+9310G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441652 | |||||||
| chr12:5441693 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0044 |
3 | HG02257.hp1 HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.18+9351C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441693 | |||||||
| chr12:5441720 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(290): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.18+9378C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441720 | |||||||
| chr12:5441723 | C | T | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+9381C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441723 | |||||||
| chr12:5441729 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.18+9387G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441729 | |||||||
| chr12:5441821 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0037 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.18+9479G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441821 | |||||||
| chr12:5441821 | G | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(245): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.18+9479G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441821 | |||||||
| chr12:5441844 | C | T | 1 | a0002c0003t0001g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18+9502C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441844 | |||||||
| chr12:5441899 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(268): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.18+9557A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5441899 | |||||||
| chr12:5442036 | A | G | 1 | a0001c0004t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.18+9694A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442036 | |||||||
| chr12:5442286 | G | A | 326 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(323): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.18+9944G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442286 | |||||||
| chr12:5442381 | G | C | 5 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0228 others(2): Show |
5 | HG00621.hp2 NA18955.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+10039G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442381 | |||||||
| chr12:5442466 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(173): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.18+10124G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442466 | |||||||
| chr12:5442467 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+10125A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442467 | |||||||
| chr12:5442476 | T | C | 34 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0065 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.18+10134T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442476 | |||||||
| chr12:5442579 | A | G | 1 | a0002c0003t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18+10237A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442579 | |||||||
| chr12:5442841 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+10499G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442841 | |||||||
| chr12:5442885 | C | T | 1 | a0001c0002t0001g0333 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.18+10543C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442885 | |||||||
| chr12:5442886 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+10544T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442886 | |||||||
| chr12:5442910 | C | G | 187 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.18+10568C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442910 | |||||||
| chr12:5442946 | G | A | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0001c0002t0001g0206 |
3 | HG01070.hp2 HG01243.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.18+10604G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442946 | |||||||
| chr12:5442960 | A | C | 24 | a0001c0001t0001g0035 a0001c0001t0001g0063 a0001c0001t0001g0064 others(21): Show |
24 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.18+10618A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5442960 | |||||||
| chr12:5443011 | T | C | 8 | a0001c0001t0001g0043 a0001c0001t0001g0166 a0001c0001t0002g0338 others(5): Show |
8 | HG01884.hp1 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+10669T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443011 | |||||||
| chr12:5443058 | A | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0339 a0001c0001t0004g0303 |
3 | HG03209.hp2 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.18+10716A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443058 | |||||||
| chr12:5443113 | C | T | 28 | a0001c0001t0001g0091 a0001c0001t0001g0146 a0001c0001t0001g0172 others(25): Show |
29 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.18+10771C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443113 | |||||||
| chr12:5443115 | C | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(230): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.18+10773C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443115 | |||||||
| chr12:5443132 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.18+10790C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443132 | |||||||
| chr12:5443265 | C | T | 1 | a0001c0002t0001g0332 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.18+10923C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443265 | |||||||
| chr12:5443304 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0172 a0001c0001t0001g0320 others(1): Show |
4 | NA18990.hp1 NA19012.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+10962T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443304 | |||||||
| chr12:5443503 | C | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(241): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.18+11161C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443503 | |||||||
| chr12:5443653 | T | C | 1 | a0001c0002t0001g0011 | 2 | NA18947.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.18+11311T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443653 | |||||||
| chr12:5443689 | T | G | 1 | a0001c0001t0001g0300 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.18+11347T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443689 | |||||||
| chr12:5443703 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.18+11361A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443703 | |||||||
| chr12:5443740 | A | T | 1 | a0001c0002t0001g0311 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.18+11398A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443740 | |||||||
| chr12:5443865 | G | A | 2 | a0001c0001t0001g0300 a0001c0002t0001g0269 |
2 | HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.18+11523G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443865 | |||||||
| chr12:5443895 | G | A | 56 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0158 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+11553G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5443895 | |||||||
| chr12:5444071 | TC | T | 56 | a0001c0001t0001g0109 a0001c0001t0001g0114 a0001c0001t0001g0158 others(53): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+11732delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5444071 | ||||||
| chr12:5444199 | C | T | 1 | a0001c0002t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18+11857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444199 | |||||||
| chr12:5444321 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.18+11979G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444321 | |||||||
| chr12:5444337 | G | A | 300 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(297): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.18+11995G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444337 | |||||||
| chr12:5444347 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0034 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.18+12005A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444347 | |||||||
| chr12:5444355 | T | C | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+12013T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444355 | |||||||
| chr12:5444378 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+12036G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444378 | |||||||
| chr12:5444423 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0336 |
2 | HG02071.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.18+12081C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444423 | |||||||
| chr12:5444448 | T | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0056 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+12106T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444448 | |||||||
| chr12:5444450 | G | T | 1 | a0002c0003t0001g0006 | 2 | NA18940.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.18+12108G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444450 | |||||||
| chr12:5444669 | C | CT | 7 | a0001c0001t0001g0117 a0001c0001t0001g0167 a0002c0003t0001g0057 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+12336dupT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5444669 | ||||||
| chr12:5444678 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+12336T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444678 | |||||||
| chr12:5444748 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0004g0303 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+12406C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444748 | |||||||
| chr12:5444845 | C | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(338): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.18+12503C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444845 | |||||||
| chr12:5444855 | A | T | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+12513A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5444855 | |||||||
| chr12:5445026 | C | G | 303 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(300): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.18+12684C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445026 | |||||||
| chr12:5445078 | G | T | 1 | a0001c0002t0001g0193 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.18+12736G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445078 | |||||||
| chr12:5445119 | A | G | 1 | a0002c0003t0001g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+12777A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445119 | |||||||
| chr12:5445274 | C | A | 1 | a0001c0001t0001g0019 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12932C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445274 | |||||||
| chr12:5445275 | C | A | 1 | a0001c0001t0001g0019 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12933C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445275 | |||||||
| chr12:5445276 | T | A | 1 | a0001c0001t0001g0019 | 2 | HG01106.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.18+12934T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445276 | |||||||
| chr12:5445276 | T | TG | 299 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(296): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.18+12934_18+12935i others(3): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445276 | |||||||
| chr12:5445287 | GATGTGTG others(5): Show |
G | 7 | a0001c0001t0001g0091 a0001c0001t0001g0146 a0001c0001t0001g0172 others(4): Show |
7 | HG00438.hp1 NA18966.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+12958_18+12969d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445287 | ||||||
| chr12:5445288 | A | ATG | 37 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(34): Show |
38 | HG01175.hp1 HG01255.hp1 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+12956_18+12957d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | A | ATGTG | 9 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0065 others(6): Show |
10 | HG02055.hp1 HG02074.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+12954_18+12957d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | A | ATGTGTG | 10 | a0001c0001t0001g0168 a0001c0001t0001g0222 a0001c0001t0001g0298 others(7): Show |
11 | HG00408.hp2 HG00741.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+12952_18+12957d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.18+12948_18+12957d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | A | ATGTGTGT others(5): Show |
1 | a0001c0002t0001g0335 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.18+12957_18+12958i others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | ATGTGTGT others(9): Show |
A | 2 | a0001c0002t0001g0003 a0001c0004t0001g0141 |
2 | HG02630.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.18+12958_18+12973d others(18): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445288 | ATGTGTGT others(11): Show |
A | 1 | a0001c0002t0001g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+12958_18+12975d others(20): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445288 | ||||||
| chr12:5445290 | GTGTGTGT others(3): Show |
G | 9 | a0001c0001t0001g0120 a0001c0001t0001g0233 a0001c0001t0001g0245 others(6): Show |
9 | HG00642.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12958_18+12967d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445290 | ||||||
| chr12:5445292 | GTGTGTGT others(1): Show |
G | 89 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
95 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.18+12958_18+12965d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445292 | ||||||
| chr12:5445294 | GTGTGTA | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(45): Show |
51 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.18+12958_18+12963d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445294 | ||||||
| chr12:5445296 | GTGTA | G | 37 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(34): Show |
38 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.18+12958_18+12961d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445296 | ||||||
| chr12:5445298 | GTA | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0073 a0001c0001t0001g0077 others(40): Show |
44 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.18+12958_18+12959d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5445298 | ||||||
| chr12:5445300 | A | G | 105 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(102): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.18+12958A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445300 | |||||||
| chr12:5445338 | T | G | 1 | a0002c0005t0001g0257 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.18+12996T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445338 | |||||||
| chr12:5445382 | A | T | 70 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(67): Show |
79 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.18+13040A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445382 | |||||||
| chr12:5445481 | G | A | 1 | a0002c0010t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+13139G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445481 | |||||||
| chr12:5445501 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+13159C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445501 | |||||||
| chr12:5445512 | T | G | 301 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(298): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.18+13170T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445512 | |||||||
| chr12:5445631 | G | A | 1 | a0001c0001t0002g0338 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+13289G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445631 | |||||||
| chr12:5445720 | C | T | 1 | a0001c0002t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+13378C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445720 | |||||||
| chr12:5445721 | G | A | 2 | a0001c0001t0001g0209 a0002c0003t0001g0207 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.18+13379G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445721 | |||||||
| chr12:5445741 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.18+13399A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445741 | |||||||
| chr12:5445778 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0168 a0001c0001t0002g0338 others(4): Show |
7 | HG01884.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+13436C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445778 | |||||||
| chr12:5445874 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(211): Show |
227 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.18+13532G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445874 | |||||||
| chr12:5445954 | G | A | 23 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(20): Show |
23 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+13612G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5445954 | |||||||
| chr12:5446069 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.18+13727A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446069 | |||||||
| chr12:5446076 | T | C | 4 | a0001c0001t0001g0259 a0001c0002t0001g0151 a0001c0002t0001g0258 others(1): Show |
4 | HG02273.hp2 HG02293.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+13734T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446076 | |||||||
| chr12:5446090 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+13748T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446090 | |||||||
| chr12:5446252 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+13910C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446252 | |||||||
| chr12:5446330 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(1): Show |
4 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+13988A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446330 | |||||||
| chr12:5446352 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0056 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+14010C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446352 | |||||||
| chr12:5446368 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18+14026C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446368 | |||||||
| chr12:5446468 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+14126A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446468 | |||||||
| chr12:5446923 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0222 others(1): Show |
4 | HG02055.hp2 HG02723.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+14581C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5446923 | |||||||
| chr12:5447047 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0056 others(4): Show |
7 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+14705G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447047 | |||||||
| chr12:5447170 | A | C | 1 | a0001c0002t0001g0182 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.18+14828A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447170 | |||||||
| chr12:5447450 | C | T | 2 | a0001c0002t0001g0201 a0001c0002t0001g0223 |
2 | HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.18+15108C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447450 | |||||||
| chr12:5447472 | G | A | 1 | a0002c0003t0001g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.18+15130G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447472 | |||||||
| chr12:5447551 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+15209T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447551 | |||||||
| chr12:5447650 | G | T | 1 | a0002c0003t0001g0132 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.18+15308G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5447650 | |||||||
| chr12:5448041 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(64): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.18+15699G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448041 | |||||||
| chr12:5448296 | G | T | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.18+15954G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448296 | |||||||
| chr12:5448361 | G | A | 6 | a0001c0001t0001g0116 a0001c0002t0001g0119 a0001c0002t0001g0161 others(3): Show |
6 | HG00099.hp1 HG00639.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+16019G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448361 | |||||||
| chr12:5448727 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+16385G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5448727 | |||||||
| chr12:5449037 | C | A | 2 | a0001c0002t0001g0184 a0001c0009t0001g0281 |
2 | HG00673.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.18+16695C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449037 | |||||||
| chr12:5449133 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+16791G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449133 | |||||||
| chr12:5449140 | G | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+16798G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449140 | |||||||
| chr12:5449192 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+16850G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449192 | |||||||
| chr12:5449234 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.18+16892G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449234 | |||||||
| chr12:5449301 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0056 others(3): Show |
6 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+16959C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449301 | |||||||
| chr12:5449352 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+17010C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449352 | |||||||
| chr12:5449532 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+17190A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449532 | |||||||
| chr12:5449574 | G | A | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+17232G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449574 | |||||||
| chr12:5449655 | G | T | 1 | a0002c0003t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.18+17313G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449655 | |||||||
| chr12:5449907 | G | C | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.18+17565G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449907 | |||||||
| chr12:5449922 | C | G | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.18+17580C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449922 | |||||||
| chr12:5449945 | A | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(81): Show |
87 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.18+17603A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5449945 | |||||||
| chr12:5450214 | G | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(338): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.18+17872G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450214 | |||||||
| chr12:5450246 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.18+17904G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450246 | |||||||
| chr12:5450432 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+18090C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450432 | |||||||
| chr12:5450502 | A | T | 1 | a0001c0002t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.18+18160A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450502 | |||||||
| chr12:5450579 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.18+18237A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450579 | |||||||
| chr12:5450580 | T | A | 1 | a0001c0002t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+18238T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450580 | |||||||
| chr12:5450700 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+18358A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450700 | |||||||
| chr12:5450728 | G | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(344): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.18+18386G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450728 | |||||||
| chr12:5450851 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+18509C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450851 | |||||||
| chr12:5450855 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.18+18513G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450855 | |||||||
| chr12:5450856 | G | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(338): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.18+18514G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450856 | |||||||
| chr12:5450992 | C | T | 74 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
83 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.18+18650C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5450992 | |||||||
| chr12:5451283 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+18941C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451283 | |||||||
| chr12:5451284 | T | G | 1 | a0001c0001t0001g0324 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.18+18942T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451284 | |||||||
| chr12:5451416 | C | T | 2 | a0001c0002t0001g0195 a0001c0002t0001g0202 |
2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.18+19074C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451416 | |||||||
| chr12:5451459 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0112 others(3): Show |
6 | HG02055.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+19117A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451459 | |||||||
| chr12:5451476 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0056 a0001c0001t0001g0112 others(3): Show |
6 | HG02055.hp2 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+19134G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451476 | |||||||
| chr12:5451714 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0112 others(2): Show |
5 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+19372A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451714 | |||||||
| chr12:5451732 | G | C | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(328): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.18+19390G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451732 | |||||||
| chr12:5451813 | C | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0135 others(1): Show |
4 | HG00280.hp1 HG01261.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+19471C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451813 | |||||||
| chr12:5451980 | A | G | 1 | a0001c0002t0001g0249 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.18+19638A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5451980 | |||||||
| chr12:5452034 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(138): Show |
145 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.18+19692T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452034 | |||||||
| chr12:5452096 | CT | C | 91 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0043 others(88): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.18+19771delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5452096 | ||||||
| chr12:5452096 | CTT | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(243): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.18+19770_18+19771d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5452096 | ||||||
| chr12:5452119 | C | T | 4 | a0001c0002t0001g0007 a0001c0002t0001g0031 a0001c0002t0001g0098 others(1): Show |
5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+19777C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452119 | |||||||
| chr12:5452120 | G | A | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18+19778G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452120 | |||||||
| chr12:5452139 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0105 |
2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.18+19797G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452139 | |||||||
| chr12:5452252 | C | T | 1 | a0001c0002t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.18+19910C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452252 | |||||||
| chr12:5452253 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0222 a0002c0003t0001g0169 |
3 | HG02055.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+19911G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452253 | |||||||
| chr12:5452483 | G | T | 42 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0138 others(39): Show |
47 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.18+20141G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452483 | |||||||
| chr12:5452699 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0319 a0001c0002t0001g0036 |
3 | HG00738.hp2 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.18+20357G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452699 | |||||||
| chr12:5452756 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0222 a0002c0003t0001g0169 |
3 | HG02055.hp2 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+20414T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452756 | |||||||
| chr12:5452771 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+20429A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452771 | |||||||
| chr12:5452853 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.18+20511G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452853 | |||||||
| chr12:5452938 | A | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0319 a0001c0002t0001g0036 |
3 | HG00738.hp2 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.18+20596A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452938 | |||||||
| chr12:5452956 | G | A | 24 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0093 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+20614G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452956 | |||||||
| chr12:5452983 | C | G | 2 | a0002c0003t0001g0314 a0002c0003t0001g0315 |
2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.18+20641C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5452983 | |||||||
| chr12:5453117 | T | C | 24 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0055 others(21): Show |
25 | HG00099.hp2 HG00280.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.18+20775T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453117 | |||||||
| chr12:5453135 | G | T | 1 | a0002c0010t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.18+20793G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453135 | |||||||
| chr12:5453178 | G | A | 41 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0138 others(38): Show |
46 | HG00323.hp2 HG00558.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.18+20836G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453178 | |||||||
| chr12:5453366 | C | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0341 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.18+21024C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453366 | |||||||
| chr12:5453408 | T | C | 1 | a0001c0006t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+21066T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453408 | |||||||
| chr12:5453521 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.18+21179C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453521 | |||||||
| chr12:5453546 | C | T | 1 | a0001c0006t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+21204C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453546 | |||||||
| chr12:5453552 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+21210G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453552 | |||||||
| chr12:5453659 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.18+21317G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453659 | |||||||
| chr12:5453701 | C | T | 27 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0112 others(24): Show |
32 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.18+21359C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453701 | |||||||
| chr12:5453895 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0168 a0001c0002t0001g0041 others(4): Show |
7 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+21553C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453895 | |||||||
| chr12:5453996 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(120): Show |
126 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.18+21654A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5453996 | |||||||
| chr12:5454001 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(117): Show |
123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.18+21659G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454001 | |||||||
| chr12:5454061 | G | C | 4 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0060 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+21719G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454061 | |||||||
| chr12:5454199 | C | CTAGCCTC others(3): Show |
1 | a0001c0001t0001g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.18+21868_18+21877d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5454199 | ||||||
| chr12:5454343 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(319): Show |
341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.18+22001A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454343 | |||||||
| chr12:5454516 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.18+22174G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454516 | |||||||
| chr12:5454725 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+22383C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454725 | |||||||
| chr12:5454779 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.18+22437C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454779 | |||||||
| chr12:5454806 | T | G | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+22464T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5454806 | |||||||
| chr12:5455022 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.18+22680A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455022 | |||||||
| chr12:5455114 | C | A | 2 | a0001c0001t0001g0189 a0002c0003t0001g0107 |
2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.18+22772C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455114 | |||||||
| chr12:5455227 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.18+22885G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455227 | |||||||
| chr12:5455291 | A | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0186 |
2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+22949A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455291 | |||||||
| chr12:5455375 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(64): Show |
76 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.18+23033G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455375 | |||||||
| chr12:5455528 | TCCCCAAC others(3): Show |
T | 1 | a0001c0002t0001g0291 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.18+23188_18+23197d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455528 | ||||||
| chr12:5455533 | A | AAC | 10 | a0001c0001t0001g0094 a0001c0001t0001g0120 a0001c0001t0001g0123 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.18+23241_18+23242d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACAC | 3 | a0001c0001t0001g0219 a0001c0002t0001g0282 a0002c0003t0001g0330 |
3 | HG00408.hp1 HG00733.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.18+23239_18+23242d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACAC | 3 | a0001c0001t0001g0043 a0001c0001t0001g0340 a0001c0002t0001g0041 |
3 | HG01952.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.18+23237_18+23242d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACACA others(1): Show |
11 | a0001c0001t0001g0044 a0001c0001t0001g0298 a0001c0002t0001g0008 others(8): Show |
12 | HG00323.hp2 HG00621.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.18+23235_18+23242d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACACA others(3): Show |
11 | a0001c0001t0001g0026 a0001c0001t0001g0112 a0001c0001t0001g0288 others(8): Show |
11 | HG00558.hp1 HG00673.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+23233_18+23242d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACACA others(5): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0008 a0001c0002t0001g0220 others(2): Show |
7 | HG01978.hp2 HG02074.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+23231_18+23242d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACACA others(7): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0168 a0001c0002t0001g0001 others(2): Show |
5 | HG01099.hp1 HG02523.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+23229_18+23242d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | A | AACACACA others(9): Show |
1 | a0001c0002t0001g0051 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.18+23227_18+23242d others(18): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AAC | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0002t0001g0103 others(4): Show |
7 | HG00280.hp1 HG01168.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+23241_18+23242d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AACAC | A | 16 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0025 others(13): Show |
17 | HG00323.hp1 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+23239_18+23242d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AACACAC | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0056 others(15): Show |
19 | HG00423.hp2 HG00642.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.18+23237_18+23242d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AACACACA others(1): Show |
A | 61 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
67 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.18+23235_18+23242d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AACACACA others(3): Show |
A | 1 | a0001c0004t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.18+23233_18+23242d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455533 | AACACACA others(5): Show |
A | 6 | a0001c0001t0001g0252 a0001c0002t0001g0014 a0001c0002t0001g0234 others(3): Show |
6 | HG00642.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+23231_18+23242d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455533 | ||||||
| chr12:5455555 | C | A | 1 | a0001c0004t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+23213C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455555 | |||||||
| chr12:5455567 | CACACACA others(11): Show |
C | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+23227_18+23244d others(20): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455567 | ||||||
| chr12:5455571 | CACACACA others(7): Show |
C | 2 | a0001c0001t0004g0303 a0001c0002t0001g0171 |
2 | HG01516.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.18+23231_18+23244d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455571 | ||||||
| chr12:5455573 | CACACACA others(5): Show |
C | 26 | a0001c0001t0001g0040 a0001c0001t0001g0158 a0001c0001t0001g0259 others(23): Show |
27 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.18+23233_18+23244d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455573 | ||||||
| chr12:5455575 | CACACACA others(3): Show |
C | 43 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0073 others(40): Show |
43 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.18+23235_18+23244d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455575 | ||||||
| chr12:5455577 | CACACACA others(1): Show |
C | 27 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0047 others(24): Show |
28 | HG01106.hp2 HG01109.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.18+23237_18+23244d others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455577 | ||||||
| chr12:5455579 | CACACAT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(26): Show |
30 | HG00423.hp1 HG01255.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+23239_18+23244d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455579 | ||||||
| chr12:5455581 | CACAT | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(34): Show |
37 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.18+23241_18+23244d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455581 | ||||||
| chr12:5455583 | CAT | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0078 others(7): Show |
10 | HG00558.hp2 HG02630.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.18+23243_18+23244d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5455583 | ||||||
| chr12:5455585 | T | C | 49 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0044 others(46): Show |
54 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.18+23243T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455585 | |||||||
| chr12:5455743 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(319): Show |
341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.18+23401A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5455743 | |||||||
| chr12:5456138 | G | A | 1 | a0001c0002t0001g0249 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.18+23796G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456138 | |||||||
| chr12:5456199 | G | A | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.18+23857G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456199 | |||||||
| chr12:5456349 | C | A | 1 | a0001c0004t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+24007C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456349 | |||||||
| chr12:5456394 | C | T | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+24052C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456394 | |||||||
| chr12:5456487 | C | A | 5 | a0001c0001t0001g0209 a0001c0004t0001g0139 a0001c0004t0001g0157 others(2): Show |
5 | HG02965.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+24145C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456487 | |||||||
| chr12:5456524 | C | T | 5 | a0002c0003t0001g0050 a0002c0003t0001g0083 a0002c0003t0001g0090 others(2): Show |
5 | HG01361.hp1 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+24182C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456524 | |||||||
| chr12:5456602 | C | T | 1 | a0002c0003t0001g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.18+24260C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456602 | |||||||
| chr12:5456620 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0142 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.18+24278C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456620 | |||||||
| chr12:5456648 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.18+24306G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456648 | |||||||
| chr12:5456708 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.18+24366C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456708 | |||||||
| chr12:5456941 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18+24599G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456941 | |||||||
| chr12:5456945 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+24603C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456945 | |||||||
| chr12:5456966 | C | T | 29 | a0001c0001t0001g0158 a0001c0001t0001g0259 a0001c0001t0001g0262 others(26): Show |
30 | HG00280.hp2 HG00733.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.18+24624C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456966 | |||||||
| chr12:5456974 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0004g0303 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.18+24632G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5456974 | |||||||
| chr12:5457046 | A | G | 1 | a0001c0002t0001g0095 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18+24704A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457046 | |||||||
| chr12:5457355 | C | T | 1 | a0001c0006t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.18+25013C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457355 | |||||||
| chr12:5457511 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.18+25169G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457511 | |||||||
| chr12:5457511 | G | C | 1 | a0001c0011t0001g0287 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.18+25169G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457511 | |||||||
| chr12:5457638 | G | A | 1 | a0001c0002t0001g0212 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.18+25296G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457638 | |||||||
| chr12:5457653 | C | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+25311C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457653 | |||||||
| chr12:5457811 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.18+25469C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457811 | |||||||
| chr12:5457960 | C | G | 1 | a0002c0003t0001g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+25618C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457960 | |||||||
| chr12:5457979 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(182): Show |
190 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.18+25637T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457979 | |||||||
| chr12:5457980 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(119): Show |
125 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.18+25638G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457980 | |||||||
| chr12:5457997 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.18+25655A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5457997 | |||||||
| chr12:5458084 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.18+25742T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458084 | |||||||
| chr12:5458139 | G | A | 1 | a0001c0004t0001g0241 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.18+25797G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458139 | |||||||
| chr12:5458215 | A | C | 321 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(318): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.18+25873A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458215 | |||||||
| chr12:5458284 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0001g0135 |
3 | HG00280.hp1 HG00741.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.18+25942C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458284 | |||||||
| chr12:5458299 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.18+25957C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458299 | |||||||
| chr12:5458410 | T | G | 7 | a0001c0002t0001g0074 a0002c0003t0001g0006 a0002c0003t0001g0049 others(4): Show |
8 | HG00423.hp1 HG02027.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.18+26068T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458410 | |||||||
| chr12:5458427 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.18+26085C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458427 | |||||||
| chr12:5458453 | A | G | 58 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0030 others(55): Show |
60 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.18+26111A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458453 | |||||||
| chr12:5458505 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+26163T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458505 | |||||||
| chr12:5458669 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.18+26327A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458669 | |||||||
| chr12:5458700 | A | G | 1 | a0001c0001t0002g0338 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.18+26358A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458700 | |||||||
| chr12:5458759 | T | C | 3 | a0001c0001t0001g0204 a0001c0004t0001g0205 a0001c0004t0001g0346 |
3 | HG01993.hp1 HG02602.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.18+26417T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458759 | |||||||
| chr12:5458891 | G | A | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.18+26549G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458891 | |||||||
| chr12:5458937 | C | A | 31 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0112 others(28): Show |
36 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.18+26595C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458937 | |||||||
| chr12:5458967 | C | G | 1 | a0001c0001t0001g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.18+26625C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5458967 | |||||||
| chr12:5459005 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(118): Show |
124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.18+26663C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459005 | |||||||
| chr12:5459054 | C | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(116): Show |
122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+26712C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459054 | |||||||
| chr12:5459126 | G | A | 4 | a0001c0002t0001g0226 a0001c0002t0001g0227 a0001c0002t0001g0228 others(1): Show |
4 | HG00621.hp2 NA18955.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+26784G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459126 | |||||||
| chr12:5459227 | T | C | 5 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0060 others(2): Show |
5 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+26885T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459227 | |||||||
| chr12:5459405 | C | T | 1 | a0001c0002t0001g0332 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.18+27063C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459405 | |||||||
| chr12:5459432 | C | T | 1 | a0001c0002t0001g0181 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.18+27090C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459432 | |||||||
| chr12:5459750 | G | A | 1 | a0002c0003t0001g0129 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.18+27408G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5459750 | |||||||
| chr12:5460053 | A | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG00099.hp2 HG01243.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.18+27711A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460053 | |||||||
| chr12:5460105 | C | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(250): Show |
270 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.18+27763C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460105 | |||||||
| chr12:5460407 | C | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(61): Show |
73 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.18+28065C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460407 | |||||||
| chr12:5460505 | A | G | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+28163A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460505 | |||||||
| chr12:5460535 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0056 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+28193C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460535 | |||||||
| chr12:5460681 | A | T | 1 | a0001c0002t0001g0200 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.18+28339A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460681 | |||||||
| chr12:5460742 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.18+28400C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460742 | |||||||
| chr12:5460782 | G | T | 1 | a0001c0002t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+28440G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460782 | |||||||
| chr12:5460802 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+28460C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460802 | |||||||
| chr12:5460842 | A | G | 3 | a0001c0002t0001g0127 a0001c0002t0001g0179 a0001c0002t0001g0180 |
3 | HG00621.hp1 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.18+28500A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5460842 | |||||||
| chr12:5461034 | C | G | 1 | a0001c0006t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.18+28692C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461034 | |||||||
| chr12:5461036 | C | T | 9 | a0001c0001t0001g0047 a0001c0001t0001g0138 a0001c0001t0001g0140 others(6): Show |
9 | HG02109.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+28694C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461036 | |||||||
| chr12:5461049 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.18+28707G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461049 | |||||||
| chr12:5461070 | G | C | 1 | a0001c0002t0001g0170 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.18+28728G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461070 | |||||||
| chr12:5461089 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(114): Show |
120 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.18+28747G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461089 | |||||||
| chr12:5461272 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0056 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+28930C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461272 | |||||||
| chr12:5461455 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0084 others(13): Show |
16 | HG00438.hp2 HG00558.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.18+29113T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461455 | |||||||
| chr12:5461580 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(1): Show |
4 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+29238A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5461580 | |||||||
| chr12:5462196 | ACTCT | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(116): Show |
122 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.18+29860_18+29863d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5462196 | ||||||
| chr12:5462282 | T | G | 64 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(61): Show |
73 | HG00140.hp2 HG00423.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.18+29940T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462282 | |||||||
| chr12:5462489 | T | C | 4 | a0001c0002t0001g0007 a0001c0002t0001g0031 a0001c0002t0001g0098 others(1): Show |
5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+30147T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462489 | |||||||
| chr12:5462570 | G | A | 2 | a0001c0001t0001g0196 a0001c0002t0001g0148 |
2 | HG03209.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.18+30228G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462570 | |||||||
| chr12:5462679 | C | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(115): Show |
121 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.18+30337C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462679 | |||||||
| chr12:5462815 | T | C | 58 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0030 others(55): Show |
60 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.18+30473T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462815 | |||||||
| chr12:5462972 | A | G | 1 | a0001c0002t0001g0194 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.18+30630A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5462972 | |||||||
| chr12:5463044 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0236 a0001c0001t0001g0246 others(5): Show |
9 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+30702C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463044 | |||||||
| chr12:5463089 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.18+30747C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463089 | |||||||
| chr12:5463205 | C | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0025 others(121): Show |
127 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.18+30863C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463205 | |||||||
| chr12:5463316 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.19-30878A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463316 | |||||||
| chr12:5463380 | T | C | 4 | a0001c0001t0001g0118 a0001c0001t0001g0337 a0001c0001t0001g0340 others(1): Show |
4 | HG01952.hp2 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-30814T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463380 | |||||||
| chr12:5463412 | A | T | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-30782A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463412 | |||||||
| chr12:5463916 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-30278A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5463916 | |||||||
| chr12:5464447 | A | T | 156 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(153): Show |
160 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.19-29747A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464447 | |||||||
| chr12:5464544 | G | T | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-29650G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464544 | |||||||
| chr12:5464607 | G | C | 19 | a0001c0001t0001g0055 a0001c0001t0001g0109 a0001c0001t0001g0239 others(16): Show |
19 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.19-29587G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464607 | |||||||
| chr12:5464845 | G | T | 54 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0063 others(51): Show |
59 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.19-29349G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5464845 | |||||||
| chr12:5465131 | G | A | 2 | a0001c0002t0001g0242 a0001c0002t0001g0266 |
2 | HG02257.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.19-29063G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465131 | |||||||
| chr12:5465254 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-28940C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465254 | |||||||
| chr12:5465310 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-28884G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465310 | |||||||
| chr12:5465335 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.19-28859C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465335 | |||||||
| chr12:5465445 | G | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG01358.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-28749G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465445 | |||||||
| chr12:5465611 | A | G | 16 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0096 others(13): Show |
17 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-28583A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465611 | |||||||
| chr12:5465845 | A | G | 4 | a0001c0001t0001g0340 a0001c0002t0001g0224 a0001c0002t0001g0342 others(1): Show |
4 | HG01952.hp2 HG02109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-28349A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465845 | |||||||
| chr12:5465861 | C | T | 55 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0034 others(52): Show |
58 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.19-28333C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465861 | |||||||
| chr12:5465944 | C | G | 1 | a0001c0006t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-28250C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5465944 | |||||||
| chr12:5466043 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.19-28151G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466043 | |||||||
| chr12:5466272 | C | T | 1 | a0001c0002t0001g0249 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.19-27922C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466272 | |||||||
| chr12:5466301 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0047 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.19-27893G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466301 | |||||||
| chr12:5466393 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(2): Show |
5 | HG01346.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-27801G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466393 | |||||||
| chr12:5466473 | G | A | 2 | a0001c0001t0001g0243 a0001c0004t0001g0244 |
2 | HG00323.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.19-27721G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466473 | |||||||
| chr12:5466798 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19-27396G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466798 | |||||||
| chr12:5466954 | C | T | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-27240C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466954 | |||||||
| chr12:5466956 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-27238G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466956 | |||||||
| chr12:5466961 | A | C | 1 | a0001c0007t0001g0211 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.19-27233A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5466961 | |||||||
| chr12:5467059 | G | A | 37 | a0001c0001t0001g0209 a0001c0001t0001g0236 a0001c0001t0001g0240 others(34): Show |
37 | HG00280.hp2 HG00423.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.19-27135G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467059 | |||||||
| chr12:5467091 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0164 |
3 | HG02886.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.19-27103G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467091 | |||||||
| chr12:5467103 | G | A | 1 | a0002c0003t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.19-27091G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467103 | |||||||
| chr12:5467198 | C | T | 1 | a0001c0002t0001g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.19-26996C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467198 | |||||||
| chr12:5467200 | A | G | 4 | a0001c0002t0001g0119 a0001c0002t0001g0161 a0001c0002t0001g0163 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26994A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467200 | |||||||
| chr12:5467203 | T | C | 4 | a0001c0002t0001g0119 a0001c0002t0001g0161 a0001c0002t0001g0163 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26991T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467203 | |||||||
| chr12:5467205 | T | G | 4 | a0001c0002t0001g0119 a0001c0002t0001g0161 a0001c0002t0001g0163 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-26989T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467205 | |||||||
| chr12:5467228 | C | CA | 29 | a0001c0001t0001g0061 a0001c0001t0001g0071 a0001c0001t0001g0077 others(26): Show |
34 | HG00280.hp2 HG00423.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.19-26931dupA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0204 others(15): Show |
20 | HG00621.hp1 HG01175.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.19-26932_19-26931d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAAA | 20 | a0001c0001t0001g0239 a0001c0002t0001g0041 a0001c0002t0001g0060 others(17): Show |
21 | HG00738.hp1 HG00741.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.19-26933_19-26931d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAAAA | 7 | a0001c0001t0001g0114 a0001c0001t0001g0246 a0001c0001t0001g0299 others(4): Show |
7 | HG00639.hp1 HG01069.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-26934_19-26931d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAAAAA | 12 | a0001c0001t0001g0109 a0001c0001t0001g0196 a0001c0001t0001g0243 others(9): Show |
12 | HG00323.hp1 HG00642.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-26935_19-26931d others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0234 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.19-26940_19-26931d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-26941_19-26931d others(13): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CA | C | 28 | a0001c0001t0001g0055 a0001c0001t0001g0078 a0001c0001t0001g0134 others(25): Show |
29 | HG00099.hp2 HG00423.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-26931delA | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAA | C | 53 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0085 others(50): Show |
54 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.19-26932_19-26931d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAA | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(30): Show |
35 | HG00558.hp2 HG00733.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.19-26933_19-26931d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAA | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0047 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-26934_19-26931d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAA | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0115 a0001c0001t0001g0138 others(4): Show |
7 | HG01169.hp1 HG01358.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-26935_19-26931d others(7): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAAA | C | 11 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0164 others(8): Show |
11 | HG01099.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-26936_19-26931d others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAAAA others(3): Show |
C | 29 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0001g0213 others(26): Show |
31 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.19-26940_19-26931d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAAAA others(4): Show |
C | 45 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
49 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.19-26941_19-26931d others(13): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-26944_19-26931d others(16): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467228 | CAAAAAAA others(8): Show |
C | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-26945_19-26931d others(17): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467228 | ||||||
| chr12:5467272 | CTTGCCAA others(10): Show |
C | 6 | a0001c0002t0001g0022 a0001c0002t0001g0226 a0001c0002t0001g0227 others(3): Show |
6 | HG00558.hp1 HG00621.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-26920_19-26904d others(19): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5467272 | ||||||
| chr12:5467304 | G | A | 28 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0001g0168 others(25): Show |
30 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-26890G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467304 | |||||||
| chr12:5467332 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0187 |
3 | NA18969.hp2 NA18982.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.19-26862C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467332 | |||||||
| chr12:5467428 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(224): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.19-26766C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467428 | |||||||
| chr12:5467657 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-26537T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467657 | |||||||
| chr12:5467777 | G | A | 41 | a0001c0001t0001g0071 a0001c0001t0001g0204 a0001c0002t0001g0001 others(38): Show |
48 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.19-26417G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467777 | |||||||
| chr12:5467943 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0113 a0001c0001t0001g0334 |
3 | HG01346.hp1 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.19-26251A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467943 | |||||||
| chr12:5467998 | C | A | 2 | a0001c0002t0001g0191 a0001c0002t0001g0332 |
2 | NA18952.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.19-26196C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5467998 | |||||||
| chr12:5468119 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-26075C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468119 | |||||||
| chr12:5468294 | C | T | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-25900C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468294 | |||||||
| chr12:5468325 | T | A | 2 | a0001c0002t0001g0194 a0001c0002t0001g0275 |
2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.19-25869T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468325 | |||||||
| chr12:5468393 | A | G | 31 | a0001c0001t0001g0043 a0001c0001t0001g0109 a0001c0001t0001g0114 others(28): Show |
32 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.19-25801A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468393 | |||||||
| chr12:5468453 | C | T | 2 | a0001c0001t0001g0283 a0002c0003t0001g0279 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.19-25741C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468453 | |||||||
| chr12:5468504 | G | A | 1 | a0002c0005t0001g0256 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.19-25690G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468504 | |||||||
| chr12:5468610 | A | G | 1 | a0002c0003t0001g0192 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.19-25584A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468610 | |||||||
| chr12:5468701 | A | G | 77 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
82 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.19-25493A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468701 | |||||||
| chr12:5468784 | C | G | 2 | a0001c0002t0001g0095 a0001c0002t0001g0347 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.19-25410C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468784 | |||||||
| chr12:5468901 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19-25293G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5468901 | |||||||
| chr12:5469153 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.19-25041G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469153 | |||||||
| chr12:5469318 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0288 a0001c0001t0001g0340 others(3): Show |
6 | HG01192.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-24876C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469318 | |||||||
| chr12:5469489 | G | A | 76 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-24705G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469489 | |||||||
| chr12:5469673 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0288 a0001c0002t0001g0039 others(1): Show |
4 | HG01192.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-24521G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5469673 | |||||||
| chr12:5470018 | G | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-24176G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470018 | |||||||
| chr12:5470039 | C | G | 1 | a0001c0004t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19-24155C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470039 | |||||||
| chr12:5470074 | G | A | 3 | a0001c0001t0001g0189 a0002c0003t0001g0057 a0002c0003t0001g0107 |
3 | HG02895.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-24120G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470074 | |||||||
| chr12:5470204 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0288 a0001c0001t0001g0340 others(3): Show |
6 | HG01192.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-23990G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470204 | |||||||
| chr12:5470310 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-23884A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470310 | |||||||
| chr12:5470337 | C | T | 1 | a0001c0002t0001g0022 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.19-23857C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470337 | |||||||
| chr12:5470454 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.19-23740T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470454 | |||||||
| chr12:5470465 | A | G | 241 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(238): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.19-23729A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470465 | |||||||
| chr12:5470473 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19-23721A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470473 | |||||||
| chr12:5470475 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.19-23719G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470475 | |||||||
| chr12:5470531 | C | T | 1 | a0002c0003t0001g0208 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19-23663C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470531 | |||||||
| chr12:5470989 | C | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0105 |
2 | HG01192.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.19-23205C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5470989 | |||||||
| chr12:5471132 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA18986.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.19-23062C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471132 | |||||||
| chr12:5471211 | G | A | 2 | a0002c0003t0001g0314 a0002c0003t0001g0315 |
2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.19-22983G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471211 | |||||||
| chr12:5471313 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-22881G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471313 | |||||||
| chr12:5471382 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.19-22812G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471382 | |||||||
| chr12:5471519 | A | T | 1 | a0002c0003t0001g0207 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.19-22675A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471519 | |||||||
| chr12:5471520 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0138 a0001c0001t0001g0140 others(3): Show |
6 | HG02280.hp1 HG02630.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-22674C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471520 | |||||||
| chr12:5471636 | G | A | 1 | a0002c0003t0001g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.19-22558G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471636 | |||||||
| chr12:5471694 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.19-22500C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471694 | |||||||
| chr12:5471713 | T | A | 1 | a0001c0002t0001g0258 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.19-22481T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471713 | |||||||
| chr12:5471720 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-22474T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471720 | |||||||
| chr12:5471739 | C | A | 1 | a0001c0001t0002g0338 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.19-22455C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471739 | |||||||
| chr12:5471812 | T | A | 1 | a0001c0004t0001g0312 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.19-22382T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471812 | |||||||
| chr12:5471867 | G | T | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-22327G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471867 | |||||||
| chr12:5471992 | G | A | 6 | a0001c0002t0001g0022 a0001c0002t0001g0226 a0001c0002t0001g0227 others(3): Show |
6 | HG00558.hp1 HG00621.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-22202G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5471992 | |||||||
| chr12:5472188 | A | T | 10 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0038 others(7): Show |
10 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-22006A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472188 | |||||||
| chr12:5472242 | C | T | 2 | a0001c0001t0001g0030 a0002c0003t0001g0310 |
2 | NA18957.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.19-21952C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472242 | |||||||
| chr12:5472271 | G | A | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-21923G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472271 | |||||||
| chr12:5472308 | A | G | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-21886A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472308 | |||||||
| chr12:5472506 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0340 |
2 | HG01952.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.19-21688G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472506 | |||||||
| chr12:5472534 | C | A | 1 | a0002c0003t0001g0317 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.19-21660C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472534 | |||||||
| chr12:5472953 | T | C | 40 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0109 others(37): Show |
41 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.19-21241T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5472953 | |||||||
| chr12:5473032 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-21162G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473032 | |||||||
| chr12:5473063 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0037 others(3): Show |
6 | HG01346.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-21131C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473063 | |||||||
| chr12:5473202 | T | C | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-20992T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473202 | |||||||
| chr12:5473387 | C | A | 1 | a0001c0002t0001g0074 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19-20807C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473387 | |||||||
| chr12:5473394 | A | G | 38 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0109 others(35): Show |
39 | HG00323.hp1 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-20800A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473394 | |||||||
| chr12:5473406 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.19-20788G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473406 | |||||||
| chr12:5473416 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0106 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-20778G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473416 | |||||||
| chr12:5473685 | A | G | 4 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0060 others(1): Show |
4 | HG02647.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-20509A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473685 | |||||||
| chr12:5473727 | G | A | 1 | a0001c0002t0001g0223 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.19-20467G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473727 | |||||||
| chr12:5473855 | C | T | 46 | a0001c0001t0001g0071 a0001c0001t0005g0217 a0001c0002t0001g0001 others(43): Show |
53 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.19-20339C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473855 | |||||||
| chr12:5473856 | A | G | 121 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(118): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.19-20338A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5473856 | |||||||
| chr12:5474001 | T | C | 2 | a0002c0003t0001g0058 a0002c0003t0001g0345 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.19-20193T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474001 | |||||||
| chr12:5474077 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-20117G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474077 | |||||||
| chr12:5474408 | G | A | 1 | a0001c0002t0001g0282 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.19-19786G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474408 | |||||||
| chr12:5474439 | C | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0324 a0001c0001t0001g0326 others(1): Show |
5 | HG02071.hp1 HG02523.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-19755C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474439 | |||||||
| chr12:5474454 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.19-19740G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474454 | |||||||
| chr12:5474577 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.19-19617A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474577 | |||||||
| chr12:5474671 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-19523G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474671 | |||||||
| chr12:5474773 | G | A | 245 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.19-19421G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474773 | |||||||
| chr12:5474978 | A | T | 1 | a0001c0002t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.19-19216A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474978 | |||||||
| chr12:5474989 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19-19205T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5474989 | |||||||
| chr12:5475214 | G | A | 4 | a0002c0005t0001g0255 a0002c0005t0001g0256 a0002c0005t0001g0257 others(1): Show |
4 | NA18952.hp1 NA18959.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-18980G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475214 | |||||||
| chr12:5475479 | A | G | 2 | a0001c0004t0001g0139 a0001c0004t0001g0157 |
2 | HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.19-18715A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475479 | |||||||
| chr12:5475565 | TG | T | 8 | a0001c0001t0005g0217 a0001c0002t0001g0041 a0001c0002t0001g0042 others(5): Show |
8 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-18627delG | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475565 | ||||||
| chr12:5475728 | G | C | 1 | a0001c0001t0001g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.19-18466G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475728 | |||||||
| chr12:5475854 | A | AAG | 73 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(70): Show |
81 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.19-18318_19-18317d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | ||||||
| chr12:5475854 | A | AAGAG | 3 | a0001c0001t0001g0341 a0001c0002t0001g0242 a0001c0002t0001g0290 |
3 | HG02257.hp2 HG02258.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.19-18320_19-18317d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | ||||||
| chr12:5475854 | AAG | A | 5 | a0001c0002t0001g0126 a0001c0002t0001g0173 a0001c0002t0001g0177 others(2): Show |
5 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-18318_19-18317d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | ||||||
| chr12:5475854 | AAGAG | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0037 others(6): Show |
9 | HG01346.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-18320_19-18317d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475854 | ||||||
| chr12:5475898 | G | GAGAA | 8 | a0001c0001t0005g0217 a0001c0002t0001g0041 a0001c0002t0001g0042 others(5): Show |
8 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-18280_19-18277d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475898 | ||||||
| chr12:5475898 | GAGAA | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0061 a0001c0001t0001g0106 others(3): Show |
6 | HG01109.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-18280_19-18277d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475898 | ||||||
| chr12:5475915 | AGAG | A | 78 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.19-18278_19-18276d others(5): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475915 | |||||||
| chr12:5475924 | GAGAGAAA others(5): Show |
G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0037 others(3): Show |
6 | HG01346.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-18261_19-18250d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5475924 | ||||||
| chr12:5475985 | A | G | 246 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(243): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.19-18209A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5475985 | |||||||
| chr12:5476036 | G | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0038 others(7): Show |
10 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-18158G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476036 | |||||||
| chr12:5476071 | G | A | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-18123G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476071 | |||||||
| chr12:5476149 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-18045G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476149 | |||||||
| chr12:5476489 | T | C | 2 | a0001c0001t0001g0015 a0002c0003t0001g0015 |
2 | NA18981.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.19-17705T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476489 | |||||||
| chr12:5476560 | T | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-17634T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476560 | |||||||
| chr12:5476692 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-17502A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476692 | |||||||
| chr12:5476882 | T | C | 1 | a0001c0002t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.19-17312T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5476882 | |||||||
| chr12:5477085 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-17109T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477085 | |||||||
| chr12:5477139 | T | A | 80 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(77): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.19-17055T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477139 | |||||||
| chr12:5477378 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-16816A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477378 | |||||||
| chr12:5477509 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0097 a0001c0001t0001g0116 |
3 | HG00280.hp1 HG00741.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.19-16685C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477509 | |||||||
| chr12:5477686 | G | C | 1 | a0001c0002t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-16508G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477686 | |||||||
| chr12:5477744 | T | C | 1 | a0001c0006t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-16450T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477744 | |||||||
| chr12:5477819 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.19-16375G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477819 | |||||||
| chr12:5477986 | T | G | 76 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(73): Show |
84 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.19-16208T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5477986 | |||||||
| chr12:5478050 | A | C | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-16144A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478050 | |||||||
| chr12:5478151 | A | T | 49 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(46): Show |
53 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.19-16043A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478151 | |||||||
| chr12:5478173 | C | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0178 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.19-16021C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478173 | |||||||
| chr12:5478317 | T | G | 78 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(75): Show |
86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15877T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478317 | |||||||
| chr12:5478424 | C | A | 2 | a0002c0003t0001g0053 a0002c0003t0001g0054 |
2 | HG00408.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.19-15770C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478424 | |||||||
| chr12:5478476 | TC | T | 76 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(73): Show |
84 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.19-15714delC | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5478476 | ||||||
| chr12:5478517 | G | A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0037 others(5): Show |
8 | HG01346.hp1 HG01884.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-15677G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478517 | |||||||
| chr12:5478586 | T | C | 1 | a0001c0002t0001g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-15608T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478586 | |||||||
| chr12:5478587 | C | T | 78 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(75): Show |
86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15607C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478587 | |||||||
| chr12:5478588 | A | G | 78 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(75): Show |
86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15606A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478588 | |||||||
| chr12:5478761 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-15433G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478761 | |||||||
| chr12:5478764 | C | T | 2 | a0001c0004t0001g0270 a0001c0004t0001g0273 |
2 | HG01261.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.19-15430C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478764 | |||||||
| chr12:5478852 | G | A | 78 | a0001c0001t0001g0043 a0001c0001t0001g0047 a0001c0001t0001g0071 others(75): Show |
86 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-15342G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478852 | |||||||
| chr12:5478891 | A | C | 3 | a0001c0001t0001g0189 a0002c0003t0001g0057 a0002c0003t0001g0107 |
3 | HG02895.hp2 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.19-15303A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478891 | |||||||
| chr12:5478963 | C | T | 22 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(19): Show |
22 | HG00099.hp1 HG00639.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.19-15231C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5478963 | |||||||
| chr12:5479148 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.19-15046C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479148 | |||||||
| chr12:5479188 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-15006G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479188 | |||||||
| chr12:5479220 | G | C | 1 | a0001c0001t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-14974G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479220 | |||||||
| chr12:5479375 | G | A | 1 | a0001c0002t0001g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.19-14819G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479375 | |||||||
| chr12:5479426 | T | G | 80 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0047 others(77): Show |
88 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.19-14768T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479426 | |||||||
| chr12:5479506 | G | A | 28 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0001g0168 others(25): Show |
30 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-14688G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479506 | |||||||
| chr12:5479785 | C | T | 164 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.19-14409C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479785 | |||||||
| chr12:5479805 | A | C | 74 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(71): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.19-14389A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479805 | |||||||
| chr12:5479833 | T | C | 238 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(235): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.19-14361T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479833 | |||||||
| chr12:5479839 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.19-14355T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479839 | |||||||
| chr12:5479863 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.19-14331A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5479863 | |||||||
| chr12:5480106 | C | G | 40 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(37): Show |
43 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.19-14088C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480106 | |||||||
| chr12:5480125 | C | T | 174 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(171): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.19-14069C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480125 | |||||||
| chr12:5480243 | A | G | 146 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(143): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.19-13951A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480243 | |||||||
| chr12:5480487 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.19-13707C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480487 | |||||||
| chr12:5480528 | G | T | 1 | a0002c0003t0001g0006 | 2 | NA18940.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.19-13666G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480528 | |||||||
| chr12:5480530 | A | G | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-13664A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480530 | |||||||
| chr12:5480649 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-13545A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480649 | |||||||
| chr12:5480658 | G | A | 3 | a0001c0002t0001g0036 a0001c0002t0001g0095 a0001c0002t0001g0347 |
3 | HG00140.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.19-13536G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480658 | |||||||
| chr12:5480727 | C | G | 41 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(38): Show |
44 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.19-13467C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480727 | |||||||
| chr12:5480748 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-13446G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480748 | |||||||
| chr12:5480862 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-13332A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480862 | |||||||
| chr12:5480904 | A | C | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-13290A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5480904 | |||||||
| chr12:5481049 | A | G | 1 | a0001c0002t0001g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.19-13145A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481049 | |||||||
| chr12:5481347 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-12847C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481347 | |||||||
| chr12:5481478 | T | C | 162 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(159): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.19-12716T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481478 | |||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
2 | a0001c0001t0001g0112 a0001c0002t0001g0249 |
2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(564): Show |
2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(573): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
5 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(2): Show |
5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
14 | a0001c0001t0001g0094 a0001c0001t0001g0115 a0001c0001t0001g0133 others(11): Show |
14 | HG00099.hp2 HG01243.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(549): Show |
1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(558): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(518): Show |
2 | a0002c0003t0001g0053 a0002c0003t0001g0054 |
2 | HG00408.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(527): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(568): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0339 |
2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.19-12707_19-12706i others(577): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(566): Show |
1 | a0001c0002t0001g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(566): Show |
1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(547): Show |
1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(556): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(566): Show |
131 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(566): Show |
1 | a0001c0001t0001g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19-12707_19-12706i others(575): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(450): Show |
1 | a0001c0002t0001g0184 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.19-12707_19-12706i others(459): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481483 | G | GCACATAC others(450): Show |
27 | a0001c0001t0001g0026 a0001c0001t0001g0142 a0001c0001t0001g0219 others(24): Show |
29 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.19-12707_19-12706i others(459): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481483 | ||||||
| chr12:5481506 | C | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(56): Show |
63 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.19-12688C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481506 | |||||||
| chr12:5481507 | C | G | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-12687C>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481507 | |||||||
| chr12:5481576 | C | T | 136 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(133): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.19-12618C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481576 | |||||||
| chr12:5481626 | T | C | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12568T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481626 | |||||||
| chr12:5481637 | A | ACACATAC others(16): Show |
2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12557_19-12556i others(25): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481637 | |||||||
| chr12:5481637 | A | ACACT | 162 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(159): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.19-12557_19-12556i others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481637 | |||||||
| chr12:5481638 | T | C | 164 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.19-12556T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481638 | |||||||
| chr12:5481638 | T | TACTC | 51 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(48): Show |
54 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.19-12554_19-12553i others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481638 | ||||||
| chr12:5481662 | A | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12532A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481662 | |||||||
| chr12:5481713 | C | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12481C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481713 | |||||||
| chr12:5481754 | A | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0340 a0001c0001t0001g0341 |
3 | HG01952.hp2 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.19-12440A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481754 | |||||||
| chr12:5481809 | G | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0218 others(4): Show |
9 | HG02071.hp1 HG02523.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-12385G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481809 | |||||||
| chr12:5481860 | A | AACAT | 164 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(161): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.19-12330_19-12327d others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481860 | ||||||
| chr12:5481872 | C | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12322C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481872 | |||||||
| chr12:5481940 | G | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12254G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481940 | |||||||
| chr12:5481962 | C | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-12232C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5481962 | |||||||
| chr12:5481990 | G | GGCATACA others(5): Show |
1 | a0001c0001t0001g0329 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-12196_19-12185d others(14): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5481990 | ||||||
| chr12:5482099 | T | C | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-12095T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482099 | |||||||
| chr12:5482109 | C | T | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-12085C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482109 | |||||||
| chr12:5482159 | C | T | 26 | a0001c0001t0001g0219 a0001c0002t0001g0008 a0001c0002t0001g0009 others(23): Show |
28 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-12035C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482159 | |||||||
| chr12:5482174 | G | A | 2 | a0001c0002t0001g0226 a0002c0003t0001g0314 |
2 | NA18971.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.19-12020G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482174 | |||||||
| chr12:5482175 | C | T | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-12019C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482175 | |||||||
| chr12:5482213 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-11981C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482213 | |||||||
| chr12:5482265 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.19-11929G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482265 | |||||||
| chr12:5482313 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19-11881G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482313 | |||||||
| chr12:5482436 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.19-11758G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482436 | |||||||
| chr12:5482561 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-11633G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482561 | |||||||
| chr12:5482653 | A | G | 156 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(153): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.19-11541A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482653 | |||||||
| chr12:5482763 | G | C | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-11431G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482763 | |||||||
| chr12:5482941 | G | A | 1 | a0001c0002t0001g0170 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.19-11253G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5482941 | |||||||
| chr12:5483087 | ATC | A | 3 | a0001c0001t0001g0252 a0001c0002t0001g0234 a0001c0002t0001g0235 |
3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.19-11098_19-11097d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483087 | ||||||
| chr12:5483180 | T | G | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-11014T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483180 | |||||||
| chr12:5483199 | A | ATC | 43 | a0001c0001t0001g0071 a0001c0001t0001g0300 a0001c0002t0001g0001 others(40): Show |
50 | HG00423.hp2 HG00621.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.19-10973_19-10972d others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483199 | ||||||
| chr12:5483199 | A | ATCTCTCT others(3): Show |
1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-10981_19-10972d others(12): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5483199 | ||||||
| chr12:5483307 | G | A | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10887G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483307 | |||||||
| chr12:5483370 | C | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10824C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483370 | |||||||
| chr12:5483540 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-10654G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483540 | |||||||
| chr12:5483556 | G | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10638G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483556 | |||||||
| chr12:5483689 | A | G | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10505A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483689 | |||||||
| chr12:5483828 | G | C | 1 | a0002c0003t0001g0054 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.19-10366G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483828 | |||||||
| chr12:5483962 | C | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10232C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5483962 | |||||||
| chr12:5484002 | A | G | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10192A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484002 | |||||||
| chr12:5484035 | T | C | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-10159T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484035 | |||||||
| chr12:5484155 | G | A | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-10039G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484155 | |||||||
| chr12:5484198 | G | T | 2 | a0001c0001t0001g0337 a0002c0003t0001g0169 |
2 | HG02717.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.19-9996G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484198 | |||||||
| chr12:5484239 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-9955T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484239 | |||||||
| chr12:5484355 | C | T | 2 | a0001c0001t0001g0112 a0001c0002t0001g0249 |
2 | HG01169.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-9839C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484355 | |||||||
| chr12:5484515 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.19-9679A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484515 | |||||||
| chr12:5484561 | G | C | 58 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
62 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.19-9633G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484561 | |||||||
| chr12:5484586 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.19-9608A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484586 | |||||||
| chr12:5484598 | A | G | 21 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(18): Show |
21 | HG01358.hp2 HG01891.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.19-9596A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484598 | |||||||
| chr12:5484676 | C | A | 1 | a0002c0003t0001g0169 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.19-9518C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484676 | |||||||
| chr12:5484753 | T | C | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-9441T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484753 | |||||||
| chr12:5484842 | C | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-9352C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484842 | |||||||
| chr12:5484937 | A | G | 151 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(148): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.19-9257A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484937 | |||||||
| chr12:5484993 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.19-9201C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5484993 | |||||||
| chr12:5485097 | G | T | 3 | a0001c0002t0001g0153 a0001c0002t0001g0248 a0001c0002t0001g0265 |
3 | HG00280.hp2 HG01175.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.19-9097G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485097 | |||||||
| chr12:5485145 | T | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-9049T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485145 | |||||||
| chr12:5485159 | C | A | 152 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(149): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.19-9035C>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485159 | |||||||
| chr12:5485237 | C | T | 152 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(149): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.19-8957C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485237 | |||||||
| chr12:5485323 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-8871G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485323 | |||||||
| chr12:5485340 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0005g0217 |
2 | HG01358.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.19-8854T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485340 | |||||||
| chr12:5485427 | T | C | 152 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(149): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.19-8767T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485427 | |||||||
| chr12:5485432 | C | T | 145 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(142): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.19-8762C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485432 | |||||||
| chr12:5485461 | C | T | 145 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(142): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.19-8733C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485461 | |||||||
| chr12:5485556 | G | A | 134 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.19-8638G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485556 | |||||||
| chr12:5485714 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.19-8480C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485714 | |||||||
| chr12:5485794 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.19-8400G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485794 | |||||||
| chr12:5485822 | A | C | 3 | a0001c0001t0001g0243 a0001c0004t0001g0244 a0001c0004t0001g0286 |
3 | HG00323.hp1 HG02148.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.19-8372A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485822 | |||||||
| chr12:5485827 | C | T | 134 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.19-8367C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5485827 | |||||||
| chr12:5486269 | A | G | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-7925A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486269 | |||||||
| chr12:5486287 | C | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG02055.hp1 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-7907C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486287 | |||||||
| chr12:5486508 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0167 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-7686C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486508 | |||||||
| chr12:5486539 | A | G | 4 | a0002c0003t0001g0013 a0002c0003t0001g0131 a0002c0003t0001g0192 others(1): Show |
5 | NA18944.hp2 NA18946.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-7655A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486539 | |||||||
| chr12:5486581 | G | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-7613G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486581 | |||||||
| chr12:5486779 | G | A | 1 | a0001c0002t0001g0333 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.19-7415G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486779 | |||||||
| chr12:5486832 | T | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0168 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.19-7362T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486832 | |||||||
| chr12:5486880 | G | GGT | 26 | a0001c0001t0001g0026 a0001c0001t0001g0076 a0001c0001t0001g0096 others(23): Show |
27 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.19-7275_19-7274dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | G | GGTGT | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(27): Show |
33 | HG00099.hp2 HG00639.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.19-7277_19-7274dup others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | G | GGTGTGT | 3 | a0001c0001t0001g0100 a0001c0006t0001g0010 a0002c0003t0001g0314 |
4 | HG01168.hp1 HG01169.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-7279_19-7274dup others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.19-7283_19-7274dup others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | GGT | G | 9 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0341 others(6): Show |
9 | HG01070.hp2 HG02258.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-7275_19-7274del others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | GGTGT | G | 29 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
30 | HG00733.hp2 HG01081.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-7277_19-7274del others(4): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | GGTGTGT | G | 68 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0047 others(65): Show |
75 | HG00423.hp2 HG00621.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.19-7279_19-7274del others(6): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | GGTGTGTG others(1): Show |
G | 81 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(78): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.19-7281_19-7274del others(8): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486880 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0001g0029 a0001c0001t0005g0217 a0001c0002t0001g0224 |
3 | HG02109.hp1 NA19030.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.19-7283_19-7274del others(10): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5486880 | ||||||
| chr12:5486969 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(2): Show |
5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-7225G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486969 | |||||||
| chr12:5486975 | G | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-7219G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5486975 | |||||||
| chr12:5487136 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.19-7058T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487136 | |||||||
| chr12:5487180 | T | C | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-7014T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487180 | |||||||
| chr12:5487249 | G | A | 58 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(55): Show |
62 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.19-6945G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487249 | |||||||
| chr12:5487288 | C | T | 134 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(131): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.19-6906C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487288 | |||||||
| chr12:5487412 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.19-6782G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487412 | |||||||
| chr12:5487544 | T | G | 10 | a0001c0001t0001g0115 a0001c0001t0005g0217 a0001c0002t0001g0041 others(7): Show |
10 | HG01358.hp2 HG02451.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-6650T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487544 | |||||||
| chr12:5487640 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0167 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6554G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487640 | |||||||
| chr12:5487646 | T | C | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-6548T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487646 | |||||||
| chr12:5487673 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.19-6521G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487673 | |||||||
| chr12:5487773 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.19-6421C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487773 | |||||||
| chr12:5487827 | T | C | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-6367T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487827 | |||||||
| chr12:5487851 | A | G | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-6343A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487851 | |||||||
| chr12:5487868 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.19-6326C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487868 | |||||||
| chr12:5487918 | G | A | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-6276G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487918 | |||||||
| chr12:5487925 | G | T | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-6269G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5487925 | |||||||
| chr12:5488039 | T | A | 153 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(150): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.19-6155T>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488039 | |||||||
| chr12:5488074 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-6120C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488074 | |||||||
| chr12:5488075 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.19-6119A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488075 | |||||||
| chr12:5488175 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0167 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-6019C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488175 | |||||||
| chr12:5488215 | T | C | 158 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(155): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.19-5979T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488215 | |||||||
| chr12:5488357 | G | C | 4 | a0001c0001t0001g0071 a0001c0002t0001g0048 a0001c0002t0001g0185 others(1): Show |
4 | HG02135.hp1 NA18949.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-5837G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488357 | |||||||
| chr12:5488728 | G | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0044 others(4): Show |
7 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5466G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488728 | |||||||
| chr12:5488833 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.19-5361G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488833 | |||||||
| chr12:5488881 | T | C | 1 | a0001c0002t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.19-5313T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5488881 | |||||||
| chr12:5489066 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-5128A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489066 | |||||||
| chr12:5489129 | G | A | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0167 others(4): Show |
7 | HG01891.hp2 HG02109.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5065G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489129 | |||||||
| chr12:5489215 | A | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0289 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.19-4979A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489215 | |||||||
| chr12:5489387 | C | T | 9 | a0001c0001t0001g0115 a0001c0001t0005g0217 a0001c0002t0001g0041 others(6): Show |
9 | HG01358.hp2 HG02451.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-4807C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489387 | |||||||
| chr12:5489415 | T | C | 1 | a0001c0006t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.19-4779T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489415 | |||||||
| chr12:5489437 | AG | A | 7 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0060 others(4): Show |
7 | HG02451.hp2 HG02647.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-4755delG | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5489437 | ||||||
| chr12:5489629 | A | C | 7 | a0001c0001t0001g0114 a0001c0001t0001g0246 a0001c0002t0001g0237 others(4): Show |
8 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.19-4565A>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489629 | |||||||
| chr12:5489676 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4518T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489676 | |||||||
| chr12:5489716 | G | A | 1 | a0001c0002t0001g0344 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19-4478G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489716 | |||||||
| chr12:5489799 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4395A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489799 | |||||||
| chr12:5489851 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-4343A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489851 | |||||||
| chr12:5489924 | G | A | 6 | a0002c0003t0001g0050 a0002c0003t0001g0083 a0002c0003t0001g0089 others(3): Show |
6 | HG01257.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-4270G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5489924 | |||||||
| chr12:5490141 | T | C | 2 | a0001c0002t0001g0234 a0001c0002t0001g0235 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.19-4053T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490141 | |||||||
| chr12:5490231 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.19-3963G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490231 | |||||||
| chr12:5490272 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-3922G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490272 | |||||||
| chr12:5490480 | T | C | 141 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(138): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.19-3714T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490480 | |||||||
| chr12:5490501 | C | T | 1 | a0001c0002t0001g0266 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.19-3693C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490501 | |||||||
| chr12:5490590 | C | T | 2 | a0001c0001t0001g0243 a0001c0004t0001g0286 |
2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.19-3604C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490590 | |||||||
| chr12:5490736 | G | C | 139 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(136): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.19-3458G>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490736 | |||||||
| chr12:5490904 | G | A | 1 | a0001c0002t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.19-3290G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5490904 | |||||||
| chr12:5491159 | C | T | 2 | a0001c0002t0001g0159 a0001c0002t0001g0264 |
2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.19-3035C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491159 | |||||||
| chr12:5491173 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-3021C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491173 | |||||||
| chr12:5491174 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.19-3020G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491174 | |||||||
| chr12:5491300 | T | G | 65 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
69 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.19-2894T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491300 | |||||||
| chr12:5491569 | C | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0076 others(63): Show |
69 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.19-2625C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491569 | |||||||
| chr12:5491685 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.19-2509C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491685 | |||||||
| chr12:5491716 | C | CT | 82 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0038 others(79): Show |
91 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.19-2457dupT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | ||||||
| chr12:5491716 | C | CTT | 6 | a0001c0002t0001g0170 a0001c0002t0001g0178 a0001c0002t0001g0181 others(3): Show |
6 | HG00621.hp2 HG01258.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-2458_19-2457dup others(2): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | ||||||
| chr12:5491716 | CT | C | 123 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(120): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.19-2457delT | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5491716 | ||||||
| chr12:5491719 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19-2475T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491719 | |||||||
| chr12:5491740 | A | G | 338 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(335): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.19-2454A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491740 | |||||||
| chr12:5491780 | C | T | 1 | a0001c0002t0001g0275 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.19-2414C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491780 | |||||||
| chr12:5491798 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.19-2396T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491798 | |||||||
| chr12:5491845 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0031 a0001c0002t0001g0098 others(1): Show |
5 | HG00423.hp2 HG02129.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-2349G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491845 | |||||||
| chr12:5491916 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.19-2278T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491916 | |||||||
| chr12:5491975 | A | G | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01952.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.19-2219A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491975 | |||||||
| chr12:5491984 | G | T | 1 | a0001c0002t0001g0221 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.19-2210G>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491984 | |||||||
| chr12:5491994 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-2200A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491994 | |||||||
| chr12:5491996 | A | G | 342 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(339): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.19-2198A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5491996 | |||||||
| chr12:5492098 | A | G | 1 | a0001c0002t0001g0193 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.19-2096A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492098 | |||||||
| chr12:5492190 | T | C | 6 | a0001c0002t0001g0191 a0001c0002t0001g0332 a0002c0003t0001g0129 others(3): Show |
6 | HG01106.hp1 HG01255.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-2004T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492190 | |||||||
| chr12:5492233 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.19-1961A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492233 | |||||||
| chr12:5492379 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0288 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19-1815C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492379 | |||||||
| chr12:5492413 | T | C | 1 | a0001c0004t0001g0286 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19-1781T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492413 | |||||||
| chr12:5492530 | A | G | 1 | a0001c0001t0004g0303 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.19-1664A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492530 | |||||||
| chr12:5492670 | A | G | 1 | a0001c0001t0005g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19-1524A>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492670 | |||||||
| chr12:5492693 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0288 others(1): Show |
4 | HG03195.hp1 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-1501T>G | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492693 | |||||||
| chr12:5492763 | G | A | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(277): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.19-1431G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492763 | |||||||
| chr12:5492931 | C | T | 5 | a0001c0002t0001g0046 a0001c0002t0001g0068 a0001c0002t0001g0307 others(2): Show |
5 | NA18957.hp2 NA18968.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-1263C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492931 | |||||||
| chr12:5492963 | T | C | 1 | a0001c0002t0001g0295 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.19-1231T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5492963 | |||||||
| chr12:5493234 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0113 others(2): Show |
5 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-960C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493234 | |||||||
| chr12:5493352 | A | T | 4 | a0002c0003t0001g0013 a0002c0003t0001g0131 a0002c0003t0001g0192 others(1): Show |
5 | NA18944.hp2 NA18946.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-842A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493352 | |||||||
| chr12:5493484 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.19-710G>A | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493484 | |||||||
| chr12:5493653 | A | T | 1 | a0001c0001t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19-541A>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493653 | |||||||
| chr12:5493826 | T | C | 1 | a0001c0004t0001g0017 | 2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.19-368T>C | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493826 | |||||||
| chr12:5493905 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.19-289C>T | NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | chr12 | 5493905 | |||||||
| chr12:5493926 | GACCGCAG others(28): Show |
G | 1 | a0001c0001t0001g0319 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.19-264_19-230delGC others(33): Show |
NTF3 | ENSG00000185652.12 | transcript | ENST00000423158.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 5493926 |