Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23420 |
| ensemblid | ENSG00000103512.16 |
| hgncid | 30060 |
| symbol | NOMO1 |
| name | NODAL modulator 1 |
| refseq_nuc | NM_014287.4 |
| refseq_prot | NP_055102.3 |
| ensembl_nuc | ENST00000287667.12 |
| ensembl_prot | ENSP00000287667.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 14833721 |
| end | 14896157 |
| strand | + |
| ver | v1.2 |
| region | chr16:14833721-14896157 |
| region5000 | chr16:14828721-14901157 |
| regionname0 | NOMO1_chr16_14833721_14896157 |
| regionname5000 | NOMO1_chr16_14828721_14901157 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1222 | 219 | 47 | 50 | 82 | 6 | 33 | 58 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0002 | 0/0 | 1222 | 57 | 3 | 0 | 45 | 1 | 8 | 31 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0003 | 0/0 | 1222 | 21 | 6 | 0 | 15 | 0 | 0 | 14 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0004 | 0/0 | 1222 | 12 | 3 | 8 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0005 | 0/0 | 1222 | 5 | 0 | 1 | 0 | 1 | 3 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0006 | 0/0 | 1222 | 5 | 0 | 2 | 3 | 0 | 0 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0007 | 0/0 | 1222 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0008 | 0/0 | 1222 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0009 | 0/0 | 1222 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0010 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0011 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0012 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0013 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0014 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0015 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0016 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0017 | 0/0 | 1222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0018 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| a0019 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | MLVGQ others(1217): Show |
chr16 | 14828721 | 14901157 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3666 | 201 | 42 | 45 | 76 | 6 | 31 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0008 | 0/0 | 3666 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0010 | 0/0 | 3666 | 4 | 3 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0011 | 0/0 | 3666 | 3 | 1 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0013 | 0/0 | 3666 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0014 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0015 | 0/0 | 3666 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0020 | 0/0 | 3666 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0001c0021 | 0/0 | 3666 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0002c0002 | 0/0 | 3666 | 49 | 3 | 0 | 37 | 1 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0002c0005 | 0/0 | 3666 | 7 | 0 | 0 | 7 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0002c0018 | 0/0 | 3666 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0003c0003 | 0/0 | 3666 | 20 | 5 | 0 | 15 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0003c0028 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0004c0004 | 0/0 | 3666 | 12 | 3 | 8 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0005c0006 | 0/0 | 3666 | 5 | 0 | 1 | 0 | 1 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0006c0009 | 0/0 | 3666 | 5 | 0 | 2 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0007c0007 | 0/0 | 3666 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0008c0012 | 0/0 | 3666 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0009c0019 | 0/0 | 3666 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0010c0023 | 0/0 | 3666 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0011c0029 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0012c0016 | 0/0 | 3666 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0013c0027 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0014c0025 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0015c0030 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0016c0024 | 0/0 | 3666 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0017c0017 | 0/0 | 3666 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0018c0026 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 | ||
| a0019c0022 | 0/0 | 3666 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | ATGCT others(3661): Show |
chr16 | 14828721 | 14901157 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4312 | 130 | 20 | 41 | 44 | 3 | 22 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0002 | 0/1 | 4312 | 63 | 21 | 3 | 29 | 3 | 6 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0003 | 0/0 | 4313 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCGG others(4308): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0005 | 0/0 | 4312 | 2 | 0 | 0 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0006 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCGG others(4308): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0007 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0001t0008 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0008t0001 | 0/0 | 4312 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0010t0001 | 0/0 | 4312 | 4 | 3 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0011t0001 | 0/0 | 4312 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0011t0002 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0013t0001 | 0/0 | 4312 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0014t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0015t0001 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0020t0002 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0001c0021t0003 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCGG others(4308): Show |
chr16 | 14828721 | 14901157 |
| a0002c0002t0001 | 0/0 | 4312 | 46 | 0 | 0 | 37 | 1 | 8 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0002c0002t0004 | 0/0 | 4312 | 3 | 3 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0002c0005t0001 | 0/0 | 4312 | 7 | 0 | 0 | 7 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0002c0018t0001 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0003c0003t0001 | 0/0 | 4312 | 20 | 5 | 0 | 15 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0003c0028t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0004c0004t0001 | 0/0 | 4312 | 9 | 1 | 7 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0004c0004t0003 | 0/0 | 4313 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCGG others(4308): Show |
chr16 | 14828721 | 14901157 |
| a0004c0004t0009 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0005c0006t0001 | 0/0 | 4312 | 5 | 0 | 1 | 0 | 1 | 3 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0006c0009t0001 | 0/0 | 4312 | 4 | 0 | 2 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0006c0009t0003 | 0/0 | 4313 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCGG others(4308): Show |
chr16 | 14828721 | 14901157 |
| a0007c0007t0001 | 0/0 | 4312 | 5 | 0 | 0 | 5 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0008c0012t0001 | 0/0 | 4312 | 2 | 2 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0009c0019t0001 | 0/0 | 4312 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0010c0023t0002 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0011c0029t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0012c0016t0001 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0013c0027t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0014c0025t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0015c0030t0002 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0016c0024t0001 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0017c0017t0005 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0018c0026t0001 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| a0019c0022t0002 | 0/0 | 4312 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | GGCTC others(4307): Show |
chr16 | 14828721 | 14901157 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0008t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0010t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0011t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0013t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0013t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0014t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0015t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0020t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0001c0021t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0002c0018t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0003c0028t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0004c0004t0009g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0005c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0006c0009t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0007c0007t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0008c0012t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0008c0012t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0009c0019t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0010c0023t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0011c0029t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0012c0016t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0013c0027t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0014c0025t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0015c0030t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0016c0024t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0017c0017t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0018c0026t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| a0019c0022t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0280 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00140 | hp2 | a0005 | c0006 | t0001 | g0274 | EUR | GBR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0302 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0176 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0195 | EUR | FIN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00673 | hp2 | a0002 | c0005 | t0001 | g0245 | EAS | CHS | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01074 | hp1 | a0001 | c0015 | t0001 | g0254 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01074 | hp2 | a0006 | c0009 | t0001 | g0272 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01106 | hp2 | a0001 | c0013 | t0001 | g0238 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01109 | hp1 | a0004 | c0004 | t0009 | g0138 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01109 | hp2 | a0001 | c0010 | t0001 | g0019 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01255 | hp1 | a0006 | c0009 | t0001 | g0276 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01255 | hp2 | a0004 | c0004 | t0001 | g0137 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01257 | hp1 | a0001 | c0011 | t0001 | g0040 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01258 | hp2 | a0001 | c0011 | t0001 | g0039 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01358 | hp2 | a0005 | c0006 | t0001 | g0226 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01361 | hp2 | a0009 | c0019 | t0001 | g0218 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0260 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01928 | hp2 | a0004 | c0004 | t0001 | g0132 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01943 | hp1 | a0004 | c0004 | t0001 | g0140 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01952 | hp1 | a0004 | c0004 | t0001 | g0135 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01978 | hp2 | a0004 | c0004 | t0001 | g0134 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0133 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02071 | hp2 | a0001 | c0008 | t0001 | g0108 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02074 | hp2 | a0010 | c0023 | t0002 | g0199 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02145 | hp1 | a0008 | c0012 | t0001 | g0126 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0239 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02148 | hp2 | a0004 | c0004 | t0001 | g0136 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CDX | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02257 | hp1 | a0003 | c0003 | t0001 | g0026 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02451 | hp2 | a0003 | c0028 | t0001 | g0190 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02523 | hp2 | a0001 | c0008 | t0001 | g0109 | EAS | KHV | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0179 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02572 | hp2 | a0011 | c0029 | t0001 | g0263 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02602 | hp2 | a0012 | c0016 | t0001 | g0264 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02647 | hp1 | a0004 | c0004 | t0003 | g0020 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02698 | hp2 | a0001 | c0013 | t0001 | g0146 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02723 | hp1 | a0002 | c0002 | t0004 | g0141 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02723 | hp2 | a0004 | c0004 | t0003 | g0021 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02735 | hp2 | a0005 | c0006 | t0001 | g0271 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02886 | hp1 | a0001 | c0010 | t0001 | g0204 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02895 | hp1 | a0013 | c0027 | t0001 | g0125 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03098 | hp2 | a0008 | c0012 | t0001 | g0127 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03139 | hp1 | a0014 | c0025 | t0001 | g0266 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03209 | hp1 | a0015 | c0030 | t0002 | g0014 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03209 | hp2 | a0003 | c0003 | t0001 | g0128 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03239 | hp1 | a0005 | c0006 | t0001 | g0273 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03453 | hp1 | a0001 | c0014 | t0001 | g0113 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0256 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03486 | hp2 | a0001 | c0011 | t0002 | g0180 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0089 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0142 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03579 | hp2 | a0001 | c0010 | t0001 | g0201 | AFR | MSL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03654 | hp1 | a0005 | c0006 | t0001 | g0270 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0130 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03669 | hp1 | a0001 | c0020 | t0002 | g0175 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0222 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0219 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0189 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0129 | SAS | PJL | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0212 | SAS | BEB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18747 | hp1 | a0003 | c0003 | t0001 | g0102 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18946 | hp1 | a0004 | c0004 | t0001 | g0159 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18947 | hp2 | a0007 | c0007 | t0001 | g0287 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18950 | hp1 | a0006 | c0009 | t0001 | g0131 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18952 | hp2 | a0002 | c0005 | t0001 | g0228 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18956 | hp2 | a0002 | c0005 | t0001 | g0091 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18957 | hp1 | a0006 | c0009 | t0003 | g0077 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18961 | hp1 | a0001 | c0021 | t0003 | g0088 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18962 | hp1 | a0007 | c0007 | t0001 | g0017 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18963 | hp1 | a0002 | c0005 | t0001 | g0244 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18970 | hp1 | a0016 | c0024 | t0001 | g0086 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18973 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18978 | hp2 | a0007 | c0007 | t0001 | g0288 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18982 | hp1 | a0001 | c0008 | t0001 | g0046 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18983 | hp2 | a0007 | c0007 | t0001 | g0017 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18987 | hp1 | a0006 | c0009 | t0001 | g0284 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18993 | hp2 | a0017 | c0017 | t0005 | g0294 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA18999 | hp2 | a0002 | c0018 | t0001 | g0289 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19001 | hp2 | a0002 | c0005 | t0001 | g0227 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19030 | hp1 | a0018 | c0026 | t0001 | g0311 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19060 | hp1 | a0007 | c0007 | t0001 | g0286 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19060 | hp2 | a0002 | c0005 | t0001 | g0236 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19062 | hp2 | a0001 | c0008 | t0001 | g0259 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19065 | hp2 | a0001 | c0008 | t0001 | g0045 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19077 | hp2 | a0002 | c0005 | t0001 | g0229 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | YRI | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ASW | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20905 | hp2 | a0019 | c0022 | t0002 | g0186 | SAS | GIH | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG06807 | hp1 | a0001 | c0010 | t0001 | g0160 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | USA | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0258 | REF | REF | NOMO1_chr16_14828721_14901157 | NOMO1 | chr16 | 14828721 | 14901157 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14848912 | A | C | 1 | a0015 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.523A>C | p.Lys175Gln | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/31 | 654/4312 | 523/3669 | 175/1222 | chr16 | 14848912 | |||
| chr16:14863125 | G | A | 1 | a0005 | 5 | HG00140.hp2 HG01358.hp2 HG02735.hp2 others(2): Show |
missense_variant | MODERATE | c.1333G>A | p.Val445Met | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/31 | 1464/4312 | 1333/3669 | 445/1222 | chr16 | 14863125 | |||
| chr16:14864657 | A | G | 5 | a0005 a0006 a0011 others(2): Show |
13 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(10): Show |
missense_variant | MODERATE | c.1468A>G | p.Asn490Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1599/4312 | 1468/3669 | 490/1222 | chr16 | 14864657 | |||
| chr16:14864666 | A | G | 4 | a0008 a0011 a0013 others(1): Show |
5 | HG02145.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.1477A>G | p.Met493Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1608/4312 | 1477/3669 | 493/1222 | chr16 | 14864666 | |||
| chr16:14866623 | A | G | 5 | a0003 a0004 a0008 others(2): Show |
37 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(34): Show |
missense_variant | MODERATE | c.1738A>G | p.Met580Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/31 | 1869/4312 | 1738/3669 | 580/1222 | chr16 | 14866623 | |||
| chr16:14868572 | C | T | 1 | a0016 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1831C>T | p.Arg611Cys | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/31 | 1962/4312 | 1831/3669 | 611/1222 | chr16 | 14868572 | |||
| chr16:14872311 | A | C | 1 | a0010 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.2036A>C | p.Asp679Ala | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/31 | 2167/4312 | 2036/3669 | 679/1222 | chr16 | 14872311 | |||
| chr16:14875363 | C | T | 1 | a0019 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.2297C>T | p.Thr766Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/31 | 2428/4312 | 2297/3669 | 766/1222 | chr16 | 14875363 | |||
| chr16:14882663 | C | G | 1 | a0009 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.3097C>G | p.His1033Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/31 | 3228/4312 | 3097/3669 | 1033/1222 | chr16 | 14882663 | |||
| chr16:14886792 | A | G | 1 | a0007 | 5 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(2): Show |
missense_variant | MODERATE | c.3254A>G | p.Asn1085Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/31 | 3385/4312 | 3254/3669 | 1085/1222 | chr16 | 14886792 | |||
| chr16:14889192 | A | T | 1 | a0018 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3421A>T | p.Ile1141Phe | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/31 | 3552/4312 | 3421/3669 | 1141/1222 | chr16 | 14889192 | |||
| chr16:14895011 | A | G | 1 | a0017 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.3458A>G | p.Glu1153Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 30/31 | 3589/4312 | 3458/3669 | 1153/1222 | chr16 | 14895011 | |||
| chr16:14895559 | C | G | 2 | a0012 a0014 |
2 | HG02602.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.3583C>G | p.Arg1195Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3714/4312 | 3583/3669 | 1195/1222 | chr16 | 14895559 | |||
| chr16:14895563 | C | T | 4 | a0002 a0004 a0007 others(1): Show |
75 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
missense_variant | MODERATE | c.3587C>T | p.Ala1196Val | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3718/4312 | 3587/3669 | 1196/1222 | chr16 | 14895563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14844684 | C | T | 1 | a0001c0013 | 2 | HG01106.hp2 HG02698.hp2 |
synonymous_variant | LOW | c.312C>T | p.Thr104Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/31 | 443/4312 | 312/3669 | 104/1222 | chr16 | 14844684 | |||
| chr16:14846678 | C | A | 1 | a0001c0014 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.504C>A | p.Gly168Gly | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/31 | 635/4312 | 504/3669 | 168/1222 | chr16 | 14846678 | |||
| chr16:14857264 | C | T | 3 | a0001c0010 a0003c0028 a0011c0029 |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.1011C>T | p.Asn337Asn | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 10/31 | 1142/4312 | 1011/3669 | 337/1222 | chr16 | 14857264 | |||
| chr16:14864665 | C | T | 1 | a0011c0029 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1476C>T | p.Pro492Pro | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/31 | 1607/4312 | 1476/3669 | 492/1222 | chr16 | 14864665 | |||
| chr16:14872249 | C | T | 1 | a0001c0008 | 5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
synonymous_variant | LOW | c.1974C>T | p.Ile658Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/31 | 2105/4312 | 1974/3669 | 658/1222 | chr16 | 14872249 | |||
| chr16:14875367 | G | A | 1 | a0002c0005 | 7 | HG00673.hp2 NA18952.hp2 NA18956.hp2 others(4): Show |
synonymous_variant | LOW | c.2301G>A | p.Pro767Pro | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/31 | 2432/4312 | 2301/3669 | 767/1222 | chr16 | 14875367 | |||
| chr16:14876733 | G | A | 2 | a0001c0011 a0018c0026 |
4 | HG01257.hp1 HG01258.hp2 HG03486.hp2 others(1): Show |
synonymous_variant | LOW | c.2586G>A | p.Ala862Ala | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/31 | 2717/4312 | 2586/3669 | 862/1222 | chr16 | 14876733 | |||
| chr16:14878723 | A | T | 1 | a0001c0021 | 1 | NA18961.hp1 | splice_region_variant&synonymous_variant | LOW | c.2646A>T | p.Ile882Ile | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/31 | 2777/4312 | 2646/3669 | 882/1222 | chr16 | 14878723 | |||
| chr16:14878771 | C | T | 2 | a0001c0014 a0001c0020 |
2 | HG03453.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.2694C>T | p.Ser898Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/31 | 2825/4312 | 2694/3669 | 898/1222 | chr16 | 14878771 | |||
| chr16:14882656 | C | T | 1 | a0001c0008 | 5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
synonymous_variant | LOW | c.3090C>T | p.Leu1030Leu | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/31 | 3221/4312 | 3090/3669 | 1030/1222 | chr16 | 14882656 | |||
| chr16:14884476 | A | G | 2 | a0001c0020 a0002c0018 |
2 | HG03669.hp1 NA18999.hp2 |
synonymous_variant | LOW | c.3216A>G | p.Thr1072Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/31 | 3347/4312 | 3216/3669 | 1072/1222 | chr16 | 14884476 | |||
| chr16:14886856 | C | T | 1 | a0002c0018 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.3318C>T | p.Asp1106Asp | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/31 | 3449/4312 | 3318/3669 | 1106/1222 | chr16 | 14886856 | |||
| chr16:14895591 | C | T | 1 | a0001c0015 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.3615C>T | p.Ser1205Ser | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3746/4312 | 3615/3669 | 1205/1222 | chr16 | 14895591 | |||
| chr16:14895642 | T | G | 1 | a0014c0025 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.3666T>G | p.Thr1222Thr | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 3797/4312 | 3666/3669 | 1222/1222 | chr16 | 14895642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14833723 | C | CG | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0021t0003 others(2): Show |
8 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-129_-128insG | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 128 | chr16 | 14833723 | ||||||
| chr16:14833724 | T | G | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0021t0003 others(2): Show |
8 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-128T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 128 | chr16 | 14833724 | ||||||
| chr16:14833773 | G | A | 1 | a0002c0002t0004 | 3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/31 | 79 | chr16 | 14833773 | ||||||
| chr16:14895759 | C | T | 1 | a0004c0004t0009 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 114 | chr16 | 14895759 | ||||||
| chr16:14895953 | A | C | 2 | a0001c0001t0005 a0017c0017t0005 |
3 | HG03654.hp2 HG03710.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*308A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 308 | chr16 | 14895953 | ||||||
| chr16:14895970 | C | T | 1 | a0001c0001t0008 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 325 | chr16 | 14895970 | ||||||
| chr16:14895987 | G | A | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(30): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*342G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 342 | chr16 | 14895987 | ||||||
| chr16:14896090 | A | G | 1 | a0001c0001t0007 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 31/31 | 445 | chr16 | 14896090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14834057 | C | A | 1 | a0001c0010t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.165+41C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834057 | |||||||
| chr16:14834306 | C | T | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+290C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834306 | |||||||
| chr16:14834322 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+306C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834322 | |||||||
| chr16:14834360 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.165+344C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834360 | |||||||
| chr16:14834489 | C | G | 1 | a0001c0001t0001g0308 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.165+473C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834489 | |||||||
| chr16:14834533 | T | A | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+517T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834533 | |||||||
| chr16:14834687 | G | GT | 10 | a0001c0001t0001g0282 a0001c0001t0002g0277 a0001c0001t0002g0278 others(7): Show |
10 | HG00099.hp1 HG01261.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+689dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | ||||||
| chr16:14834687 | G | GTT | 24 | a0002c0002t0001g0018 a0002c0002t0001g0290 a0002c0002t0001g0291 others(21): Show |
26 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+688_165+689dup others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | ||||||
| chr16:14834687 | GT | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
133 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.165+689delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14834687 | ||||||
| chr16:14834706 | A | T | 3 | a0001c0001t0002g0285 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.165+690A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834706 | |||||||
| chr16:14834728 | T | G | 9 | a0002c0002t0001g0139 a0004c0004t0001g0132 a0004c0004t0001g0133 others(6): Show |
9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+712T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834728 | |||||||
| chr16:14834961 | G | A | 2 | a0002c0002t0004g0141 a0002c0002t0004g0142 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.165+945G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14834961 | |||||||
| chr16:14835251 | A | G | 10 | a0001c0001t0001g0275 a0004c0004t0003g0020 a0004c0004t0003g0021 others(7): Show |
10 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+1235A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835251 | |||||||
| chr16:14835365 | G | T | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+1349G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835365 | |||||||
| chr16:14835391 | G | A | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.165+1375G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835391 | |||||||
| chr16:14835416 | C | T | 1 | a0006c0009t0001g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.165+1400C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835416 | |||||||
| chr16:14835531 | C | G | 1 | a0001c0001t0002g0269 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165+1515C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835531 | |||||||
| chr16:14835754 | A | G | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | HG02257.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.165+1738A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835754 | |||||||
| chr16:14835765 | C | T | 2 | a0001c0001t0005g0129 a0001c0001t0005g0130 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.165+1749C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835765 | |||||||
| chr16:14835797 | T | C | 1 | a0002c0002t0001g0143 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.165+1781T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835797 | |||||||
| chr16:14835868 | A | G | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.165+1852A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14835868 | |||||||
| chr16:14836113 | A | C | 4 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2097A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836113 | |||||||
| chr16:14836176 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
7 | HG02027.hp2 NA18612.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+2160C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836176 | |||||||
| chr16:14836189 | G | T | 1 | a0012c0016t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165+2173G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836189 | |||||||
| chr16:14836224 | T | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.166-2183T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836224 | |||||||
| chr16:14836544 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.166-1863A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836544 | |||||||
| chr16:14836577 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.166-1830C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836577 | |||||||
| chr16:14836694 | C | CT | 12 | a0001c0001t0001g0116 a0001c0001t0001g0262 a0001c0001t0001g0308 others(9): Show |
12 | HG01255.hp1 HG01433.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-1691dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14836694 | ||||||
| chr16:14836694 | CT | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0147 others(3): Show |
6 | HG02135.hp1 HG02165.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1691delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14836694 | ||||||
| chr16:14836730 | G | A | 5 | a0002c0018t0001g0289 a0007c0007t0001g0017 a0007c0007t0001g0286 others(2): Show |
6 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-1677G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836730 | |||||||
| chr16:14836761 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-1646A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836761 | |||||||
| chr16:14836778 | T | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-1629T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836778 | |||||||
| chr16:14836809 | C | T | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.166-1598C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836809 | |||||||
| chr16:14836952 | G | A | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1455G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14836952 | |||||||
| chr16:14837021 | ATTTTG | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1381_166-1377d others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | 14837021 | ||||||
| chr16:14837134 | C | T | 1 | a0002c0002t0001g0257 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.166-1273C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837134 | |||||||
| chr16:14837155 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.166-1252C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837155 | |||||||
| chr16:14837308 | C | T | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-1099C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837308 | |||||||
| chr16:14837589 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.166-818G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837589 | |||||||
| chr16:14837688 | C | G | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.166-719C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837688 | |||||||
| chr16:14837754 | T | A | 1 | a0007c0007t0001g0286 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-653T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837754 | |||||||
| chr16:14837773 | C | T | 3 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0015t0001g0254 |
3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.166-634C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837773 | |||||||
| chr16:14837906 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.166-501A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14837906 | |||||||
| chr16:14838043 | C | A | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.166-364C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14838043 | |||||||
| chr16:14838320 | T | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0148 others(17): Show |
21 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-87T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 1/30 | chr16 | 14838320 | |||||||
| chr16:14838632 | C | T | 2 | a0002c0002t0001g0305 a0002c0002t0001g0306 |
2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.255+136C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838632 | |||||||
| chr16:14838660 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.255+164C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838660 | |||||||
| chr16:14838785 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0148 others(3): Show |
7 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+289G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838785 | |||||||
| chr16:14838848 | C | G | 1 | a0006c0009t0001g0131 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.255+352C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838848 | |||||||
| chr16:14838990 | C | G | 25 | a0002c0002t0001g0018 a0002c0002t0001g0283 a0002c0002t0001g0290 others(22): Show |
27 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.255+494C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14838990 | |||||||
| chr16:14839024 | T | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+528T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839024 | |||||||
| chr16:14839056 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.255+560T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839056 | |||||||
| chr16:14839067 | T | C | 6 | a0001c0001t0001g0275 a0005c0006t0001g0270 a0005c0006t0001g0271 others(3): Show |
6 | HG00140.hp2 HG01074.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.255+571T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839067 | |||||||
| chr16:14839159 | A | G | 1 | a0002c0002t0001g0252 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.255+663A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839159 | |||||||
| chr16:14839169 | C | T | 1 | a0002c0002t0001g0251 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.255+673C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839169 | |||||||
| chr16:14839189 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0033 others(7): Show |
11 | HG02027.hp2 HG02040.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.255+693G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839189 | |||||||
| chr16:14839334 | G | T | 1 | a0003c0003t0001g0004 | 3 | NA18973.hp2 NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.255+838G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839334 | |||||||
| chr16:14839414 | A | T | 1 | a0003c0003t0001g0110 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.255+918A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839414 | |||||||
| chr16:14839770 | G | C | 1 | a0002c0002t0001g0305 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.255+1274G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839770 | |||||||
| chr16:14839792 | A | G | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.255+1296A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839792 | |||||||
| chr16:14839850 | T | G | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.255+1354T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839850 | |||||||
| chr16:14839971 | C | G | 2 | a0001c0008t0001g0108 a0001c0008t0001g0109 |
2 | HG02071.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.256-1391C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14839971 | |||||||
| chr16:14840063 | C | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0100 others(14): Show |
23 | HG01993.hp2 HG02486.hp2 HG02717.hp1 others(20): Show |
intron_variant | MODIFIER | c.256-1299C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840063 | |||||||
| chr16:14840162 | A | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-1200A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840162 | |||||||
| chr16:14840572 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.256-790G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840572 | |||||||
| chr16:14840578 | C | T | 1 | a0001c0001t0002g0006 | 3 | NA18948.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.256-784C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840578 | |||||||
| chr16:14840592 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.256-770A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840592 | |||||||
| chr16:14840623 | G | A | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.256-739G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840623 | |||||||
| chr16:14840669 | T | C | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.256-693T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840669 | |||||||
| chr16:14840824 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.256-538G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840824 | |||||||
| chr16:14840954 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-408G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14840954 | |||||||
| chr16:14841015 | T | G | 1 | a0004c0004t0001g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.256-347T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 2/30 | chr16 | 14841015 | |||||||
| chr16:14841527 | G | A | 1 | a0001c0010t0001g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.301+120G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841527 | |||||||
| chr16:14841596 | T | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.301+189T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841596 | |||||||
| chr16:14841754 | T | A | 2 | a0002c0002t0001g0290 a0002c0002t0001g0291 |
2 | NA18971.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.301+347T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841754 | |||||||
| chr16:14841968 | C | G | 2 | a0001c0010t0001g0160 a0011c0029t0001g0263 |
2 | HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.301+561C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14841968 | |||||||
| chr16:14842223 | C | G | 4 | a0003c0003t0001g0004 a0003c0003t0001g0105 a0003c0003t0001g0106 others(1): Show |
6 | NA18973.hp2 NA18995.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+816C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842223 | |||||||
| chr16:14842251 | C | A | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.301+844C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842251 | |||||||
| chr16:14842400 | G | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(306): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.301+993G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842400 | |||||||
| chr16:14842496 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.301+1089T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842496 | |||||||
| chr16:14842513 | C | G | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+1106C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842513 | |||||||
| chr16:14842814 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.301+1407A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14842814 | |||||||
| chr16:14843011 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.301+1604G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843011 | |||||||
| chr16:14843013 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301+1606G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843013 | |||||||
| chr16:14843063 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.302-1611G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843063 | |||||||
| chr16:14843292 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.302-1382C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843292 | |||||||
| chr16:14843462 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1212G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843462 | |||||||
| chr16:14843520 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0157 |
2 | HG02040.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.302-1154G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843520 | |||||||
| chr16:14843610 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1064T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843610 | |||||||
| chr16:14843611 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1063A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843611 | |||||||
| chr16:14843612 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1062A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843612 | |||||||
| chr16:14843613 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1061A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843613 | |||||||
| chr16:14843616 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1058A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843616 | |||||||
| chr16:14843619 | A | G | 4 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1055A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843619 | |||||||
| chr16:14843631 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.302-1043T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843631 | |||||||
| chr16:14843679 | C | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0246 others(2): Show |
5 | NA18950.hp1 NA18960.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-995C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14843679 | |||||||
| chr16:14843715 | T | TTG | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(189): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.302-932_302-931dup others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | ||||||
| chr16:14843715 | T | TTGTG | 6 | a0001c0001t0001g0250 a0001c0001t0002g0162 a0001c0001t0002g0207 others(3): Show |
6 | HG00673.hp2 HG03195.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-934_302-931dup others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | ||||||
| chr16:14843715 | TTG | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
21 | HG00140.hp2 HG01074.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.302-932_302-931del others(2): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | ||||||
| chr16:14843715 | TTGTG | T | 5 | a0001c0001t0001g0098 a0003c0003t0001g0024 a0003c0003t0001g0025 others(2): Show |
5 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.302-934_302-931del others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | 14843715 | ||||||
| chr16:14844017 | G | A | 3 | a0001c0008t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0259 |
3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.302-657G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844017 | |||||||
| chr16:14844070 | G | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0047 others(8): Show |
12 | HG00323.hp2 HG00733.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.302-604G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844070 | |||||||
| chr16:14844178 | T | C | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-496T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844178 | |||||||
| chr16:14844328 | T | G | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-346T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844328 | |||||||
| chr16:14844376 | A | C | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-298A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844376 | |||||||
| chr16:14844478 | T | C | 1 | a0001c0015t0001g0254 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.302-196T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 3/30 | chr16 | 14844478 | |||||||
| chr16:14844808 | C | G | 1 | a0002c0002t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.402+34C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844808 | |||||||
| chr16:14844876 | C | T | 1 | a0008c0012t0001g0127 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.402+102C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844876 | |||||||
| chr16:14844941 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402+167G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844941 | |||||||
| chr16:14844964 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.402+190G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14844964 | |||||||
| chr16:14845014 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.402+240G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845014 | |||||||
| chr16:14845058 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.402+284G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845058 | |||||||
| chr16:14845376 | T | C | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402+602T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845376 | |||||||
| chr16:14845464 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.402+690A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845464 | |||||||
| chr16:14845487 | C | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.402+713C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845487 | |||||||
| chr16:14845531 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.402+757G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845531 | |||||||
| chr16:14845560 | T | C | 5 | a0003c0003t0001g0128 a0008c0012t0001g0126 a0008c0012t0001g0127 others(2): Show |
5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+786T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845560 | |||||||
| chr16:14845858 | C | T | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.403-719C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845858 | |||||||
| chr16:14845896 | C | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0148 others(9): Show |
13 | HG00099.hp2 HG00140.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-681C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845896 | |||||||
| chr16:14845913 | G | A | 1 | a0002c0002t0001g0307 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.403-664G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14845913 | |||||||
| chr16:14846024 | CT | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG01192.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.403-533delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 14846024 | ||||||
| chr16:14846113 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0065 others(10): Show |
16 | HG00735.hp2 HG00738.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-464G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846113 | |||||||
| chr16:14846295 | A | G | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.403-282A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846295 | |||||||
| chr16:14846323 | G | A | 14 | a0001c0001t0002g0014 a0001c0001t0002g0158 a0001c0001t0002g0164 others(11): Show |
14 | HG01496.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-254G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 4/30 | chr16 | 14846323 | |||||||
| chr16:14846912 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.509+229G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14846912 | |||||||
| chr16:14847004 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+321A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847004 | |||||||
| chr16:14847009 | T | A | 2 | a0001c0001t0002g0164 a0003c0003t0001g0099 |
2 | NA18961.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509+326T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847009 | |||||||
| chr16:14847069 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.509+386G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847069 | |||||||
| chr16:14847175 | C | T | 1 | a0004c0004t0001g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509+492C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847175 | |||||||
| chr16:14847334 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.509+651C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847334 | |||||||
| chr16:14847868 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.510-1031G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847868 | |||||||
| chr16:14847971 | T | G | 1 | a0001c0001t0002g0174 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.510-928T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14847971 | |||||||
| chr16:14848052 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.510-847A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848052 | |||||||
| chr16:14848117 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.510-782C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848117 | |||||||
| chr16:14848609 | G | A | 1 | a0001c0020t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510-290G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 5/30 | chr16 | 14848609 | |||||||
| chr16:14849896 | C | CT | 77 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(74): Show |
82 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.582+946dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14849896 | ||||||
| chr16:14849896 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
7 | HG02109.hp1 HG03139.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+946delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14849896 | ||||||
| chr16:14850002 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.582+1031C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850002 | |||||||
| chr16:14850140 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.582+1169G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850140 | |||||||
| chr16:14850156 | C | T | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.582+1185C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850156 | |||||||
| chr16:14850253 | T | C | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.582+1282T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850253 | |||||||
| chr16:14850317 | G | A | 1 | a0001c0015t0001g0254 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.582+1346G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850317 | |||||||
| chr16:14850368 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.582+1397G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850368 | |||||||
| chr16:14850374 | T | C | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.582+1403T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850374 | |||||||
| chr16:14850658 | T | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+1687T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850658 | |||||||
| chr16:14850675 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.582+1704C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850675 | |||||||
| chr16:14850740 | A | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.583-1690A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850740 | |||||||
| chr16:14850808 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.583-1622C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14850808 | |||||||
| chr16:14851083 | CA | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(243): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.583-1329delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 14851083 | ||||||
| chr16:14851231 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.583-1199G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851231 | |||||||
| chr16:14851302 | T | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.583-1128T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851302 | |||||||
| chr16:14851612 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.583-818A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851612 | |||||||
| chr16:14851739 | T | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(221): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.583-691T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14851739 | |||||||
| chr16:14852032 | A | G | 1 | a0002c0002t0001g0237 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.583-398A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852032 | |||||||
| chr16:14852058 | C | T | 1 | a0002c0005t0001g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.583-372C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852058 | |||||||
| chr16:14852059 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.583-371G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852059 | |||||||
| chr16:14852086 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.583-344G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852086 | |||||||
| chr16:14852161 | A | G | 4 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-269A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852161 | |||||||
| chr16:14852405 | A | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(44): Show |
50 | HG00323.hp2 HG00597.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.583-25A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 6/30 | chr16 | 14852405 | |||||||
| chr16:14852619 | GGTAGGAG others(19): Show |
G | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+39_735+64delTA others(24): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852619 | ||||||
| chr16:14852949 | G | A | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.735+367G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852949 | |||||||
| chr16:14852960 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.735+378A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852960 | |||||||
| chr16:14852995 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(47): Show |
54 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.735+413T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14852995 | |||||||
| chr16:14852998 | C | CA | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.735+434dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852998 | ||||||
| chr16:14852998 | CA | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(55): Show |
62 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.735+434delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | 14852998 | ||||||
| chr16:14853030 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.736-437T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853030 | |||||||
| chr16:14853201 | T | C | 1 | a0001c0008t0001g0045 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.736-266T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853201 | |||||||
| chr16:14853246 | C | G | 2 | a0002c0002t0001g0212 a0002c0002t0001g0213 |
2 | HG02523.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.736-221C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853246 | |||||||
| chr16:14853290 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.736-177T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 7/30 | chr16 | 14853290 | |||||||
| chr16:14853674 | TG | T | 14 | a0002c0002t0001g0092 a0002c0002t0001g0143 a0002c0002t0001g0211 others(11): Show |
14 | HG00597.hp1 HG03834.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.873+73delG | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr16 | 14853674 | ||||||
| chr16:14853775 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.874-162A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | chr16 | 14853775 | |||||||
| chr16:14853920 | C | G | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0008c0012t0001g0126 others(2): Show |
5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.874-17C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 8/30 | chr16 | 14853920 | |||||||
| chr16:14854332 | A | AT | 10 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0123 others(7): Show |
10 | HG01261.hp2 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+326dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14854332 | ||||||
| chr16:14854332 | AT | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0096 a0001c0001t0001g0097 others(12): Show |
15 | HG00280.hp2 HG02145.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.963+326delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14854332 | ||||||
| chr16:14854355 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.963+329G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854355 | |||||||
| chr16:14854357 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(43): Show |
49 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.963+331T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854357 | |||||||
| chr16:14854379 | A | C | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.963+353A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854379 | |||||||
| chr16:14854563 | G | A | 1 | a0001c0008t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.963+537G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854563 | |||||||
| chr16:14854644 | T | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(220): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.963+618T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854644 | |||||||
| chr16:14854747 | C | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+721C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854747 | |||||||
| chr16:14854903 | C | T | 1 | a0010c0023t0002g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+877C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854903 | |||||||
| chr16:14854982 | A | G | 2 | a0001c0001t0003g0117 a0001c0021t0003g0088 |
2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.963+956A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14854982 | |||||||
| chr16:14855059 | C | T | 1 | a0001c0013t0001g0238 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.963+1033C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855059 | |||||||
| chr16:14855342 | G | T | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.963+1316G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855342 | |||||||
| chr16:14855463 | C | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1437C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855463 | |||||||
| chr16:14855474 | T | TA | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1449dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 14855474 | ||||||
| chr16:14855653 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.964-1564A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14855653 | |||||||
| chr16:14856146 | A | G | 5 | a0003c0003t0001g0128 a0008c0012t0001g0126 a0008c0012t0001g0127 others(2): Show |
5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-1071A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856146 | |||||||
| chr16:14856224 | A | C | 9 | a0002c0002t0001g0092 a0002c0002t0001g0231 a0002c0002t0001g0232 others(6): Show |
9 | HG03834.hp1 NA18974.hp1 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.964-993A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856224 | |||||||
| chr16:14856309 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.964-908A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856309 | |||||||
| chr16:14856315 | C | A | 2 | a0002c0002t0001g0252 a0002c0002t0001g0293 |
2 | HG00597.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.964-902C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856315 | |||||||
| chr16:14856317 | G | C | 1 | a0002c0002t0001g0252 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.964-900G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856317 | |||||||
| chr16:14856444 | C | T | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-773C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856444 | |||||||
| chr16:14856709 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.964-508G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856709 | |||||||
| chr16:14856852 | T | A | 14 | a0002c0002t0001g0018 a0002c0002t0001g0283 a0002c0002t0001g0290 others(11): Show |
15 | HG00438.hp1 HG00609.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.964-365T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856852 | |||||||
| chr16:14856864 | T | C | 3 | a0002c0002t0001g0092 a0002c0002t0001g0231 a0002c0002t0001g0261 |
3 | NA18985.hp1 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.964-353T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856864 | |||||||
| chr16:14856874 | C | T | 1 | a0012c0016t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964-343C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856874 | |||||||
| chr16:14856993 | T | A | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.964-224T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14856993 | |||||||
| chr16:14857042 | G | T | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.964-175G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14857042 | |||||||
| chr16:14857110 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.964-107C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 9/30 | chr16 | 14857110 | |||||||
| chr16:14857327 | G | A | 2 | a0004c0004t0003g0020 a0004c0004t0003g0021 |
2 | HG02647.hp1 HG02723.hp2 |
splice_region_variant&intron_variant | LOW | c.1069+5G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 10/30 | chr16 | 14857327 | |||||||
| chr16:14857683 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1220+28G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14857683 | |||||||
| chr16:14857773 | CT | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(303): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1220+136delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 14857773 | ||||||
| chr16:14857921 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1220+266G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14857921 | |||||||
| chr16:14858410 | A | G | 1 | a0001c0001t0008g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1220+755A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858410 | |||||||
| chr16:14858441 | A | C | 54 | a0001c0001t0001g0114 a0001c0001t0002g0191 a0001c0001t0003g0087 others(51): Show |
56 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1220+786A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858441 | |||||||
| chr16:14858567 | C | T | 2 | a0002c0018t0001g0289 a0007c0007t0001g0286 |
2 | NA18999.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1220+912C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858567 | |||||||
| chr16:14858614 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1220+959A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858614 | |||||||
| chr16:14858651 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1220+996C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858651 | |||||||
| chr16:14858682 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0002g0191 |
2 | NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1220+1027G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858682 | |||||||
| chr16:14858837 | C | G | 1 | a0002c0002t0001g0300 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1220+1182C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14858837 | |||||||
| chr16:14859091 | C | G | 1 | a0001c0001t0002g0188 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1220+1436C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859091 | |||||||
| chr16:14859319 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1220+1664G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859319 | |||||||
| chr16:14859381 | G | A | 1 | a0002c0002t0001g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1220+1726G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859381 | |||||||
| chr16:14859590 | G | A | 3 | a0002c0002t0001g0293 a0002c0002t0001g0295 a0017c0017t0005g0294 |
3 | NA18975.hp1 NA18977.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1220+1935G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859590 | |||||||
| chr16:14859602 | C | G | 1 | a0001c0001t0002g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1220+1947C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859602 | |||||||
| chr16:14859746 | A | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0163 |
2 | HG00733.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1220+2091A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859746 | |||||||
| chr16:14859975 | G | A | 1 | a0001c0013t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1220+2320G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14859975 | |||||||
| chr16:14860176 | T | G | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1220+2521T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860176 | |||||||
| chr16:14860223 | C | T | 1 | a0002c0002t0001g0230 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1220+2568C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860223 | |||||||
| chr16:14860755 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1221-2258T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860755 | |||||||
| chr16:14860828 | A | T | 1 | a0001c0001t0002g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1221-2185A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860828 | |||||||
| chr16:14860891 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221-2122G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860891 | |||||||
| chr16:14860894 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1221-2119G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860894 | |||||||
| chr16:14860964 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1221-2049C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14860964 | |||||||
| chr16:14861506 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0149 others(1): Show |
5 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-1507G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14861506 | |||||||
| chr16:14861837 | AT | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(228): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1221-1163delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 14861837 | ||||||
| chr16:14862333 | A | G | 9 | a0002c0002t0001g0139 a0004c0004t0001g0132 a0004c0004t0001g0133 others(6): Show |
9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221-680A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862333 | |||||||
| chr16:14862387 | G | C | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1221-626G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862387 | |||||||
| chr16:14862689 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1221-324G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862689 | |||||||
| chr16:14862797 | G | C | 3 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0015t0001g0254 |
3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1221-216G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862797 | |||||||
| chr16:14862841 | G | A | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-172G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862841 | |||||||
| chr16:14862950 | T | G | 2 | a0002c0005t0001g0227 a0018c0026t0001g0311 |
2 | NA19001.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1221-63T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862950 | |||||||
| chr16:14862963 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1221-50C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 11/30 | chr16 | 14862963 | |||||||
| chr16:14863213 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0149 others(1): Show |
5 | HG00099.hp2 HG01167.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1395+26A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863213 | |||||||
| chr16:14863310 | T | G | 1 | a0001c0001t0002g0015 | 2 | HG02083.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1395+123T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863310 | |||||||
| chr16:14863592 | C | T | 2 | a0001c0001t0005g0129 a0001c0001t0005g0130 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1395+405C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863592 | |||||||
| chr16:14863663 | A | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1395+476A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863663 | |||||||
| chr16:14863951 | C | T | 5 | a0001c0008t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0108 others(2): Show |
5 | HG02071.hp2 HG02523.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1396-634C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863951 | |||||||
| chr16:14863988 | C | A | 6 | a0001c0001t0002g0268 a0003c0003t0001g0105 a0003c0003t0001g0106 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-597C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14863988 | |||||||
| chr16:14864167 | G | C | 4 | a0001c0001t0002g0268 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-418G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864167 | |||||||
| chr16:14864318 | A | G | 3 | a0001c0001t0001g0098 a0001c0014t0001g0113 a0006c0009t0001g0284 |
3 | HG03453.hp1 NA18987.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1396-267A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864318 | |||||||
| chr16:14864347 | T | C | 1 | a0009c0019t0001g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1396-238T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864347 | |||||||
| chr16:14864404 | T | C | 4 | a0001c0001t0002g0268 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-181T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864404 | |||||||
| chr16:14864453 | C | T | 8 | a0001c0001t0001g0157 a0002c0005t0001g0091 a0002c0005t0001g0227 others(5): Show |
8 | HG00673.hp2 HG02040.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1396-132C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864453 | |||||||
| chr16:14864581 | A | G | 17 | a0001c0001t0001g0053 a0001c0001t0001g0154 a0001c0001t0002g0014 others(14): Show |
17 | HG00140.hp1 HG01496.hp1 HG01884.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1396-4A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 12/30 | chr16 | 14864581 | |||||||
| chr16:14864891 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0116 |
2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1538-133A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864891 | |||||||
| chr16:14864965 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(5): Show |
8 | HG00099.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1538-59A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864965 | |||||||
| chr16:14864989 | G | A | 1 | a0001c0008t0001g0259 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1538-35G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 13/30 | chr16 | 14864989 | |||||||
| chr16:14865349 | G | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(65): Show |
76 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1669+194G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865349 | |||||||
| chr16:14865435 | G | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01993.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1669+280G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865435 | |||||||
| chr16:14865437 | G | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
19 | HG01993.hp2 HG02109.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1669+282G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865437 | |||||||
| chr16:14865551 | G | A | 12 | a0001c0001t0001g0047 a0001c0001t0001g0250 a0001c0001t0002g0205 others(9): Show |
12 | HG01109.hp2 HG01243.hp2 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.1669+396G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865551 | |||||||
| chr16:14865556 | A | G | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0016c0024t0001g0086 |
3 | HG02145.hp1 HG03098.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1669+401A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865556 | |||||||
| chr16:14865779 | T | G | 4 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669+624T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865779 | |||||||
| chr16:14865832 | G | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0054 others(27): Show |
30 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1669+677G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865832 | |||||||
| chr16:14865909 | C | G | 7 | a0001c0001t0005g0129 a0001c0001t0005g0130 a0003c0003t0001g0004 others(4): Show |
9 | HG02257.hp1 HG03130.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.1670-646C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865909 | |||||||
| chr16:14865912 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1670-643G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14865912 | |||||||
| chr16:14866065 | CT | C | 39 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(36): Show |
50 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1670-480delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 14866065 | ||||||
| chr16:14866106 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1670-449G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866106 | |||||||
| chr16:14866191 | C | T | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1670-364C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866191 | |||||||
| chr16:14866225 | A | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0003c0003t0001g0003 others(10): Show |
18 | HG01346.hp1 HG01433.hp1 HG03139.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-330A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866225 | |||||||
| chr16:14866230 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(200): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1670-325T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866230 | |||||||
| chr16:14866304 | A | C | 4 | a0002c0002t0001g0233 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-251A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866304 | |||||||
| chr16:14866305 | G | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0003c0003t0001g0003 others(10): Show |
18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-250G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866305 | |||||||
| chr16:14866305 | G | T | 4 | a0002c0002t0001g0233 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-250G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866305 | |||||||
| chr16:14866306 | T | G | 4 | a0002c0002t0001g0233 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-249T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866306 | |||||||
| chr16:14866307 | G | C | 4 | a0002c0002t0001g0233 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670-248G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866307 | |||||||
| chr16:14866307 | G | GC | 13 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0003c0003t0001g0003 others(10): Show |
18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-247dupC | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | 14866307 | ||||||
| chr16:14866312 | G | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0093 a0003c0003t0001g0003 others(10): Show |
18 | HG01109.hp1 HG01346.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670-243G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866312 | |||||||
| chr16:14866466 | G | A | 14 | a0001c0001t0001g0200 a0003c0003t0001g0003 a0003c0003t0001g0004 others(11): Show |
19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-89G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866466 | |||||||
| chr16:14866467 | A | G | 14 | a0001c0001t0001g0200 a0003c0003t0001g0003 a0003c0003t0001g0004 others(11): Show |
19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-88A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866467 | |||||||
| chr16:14866499 | G | C | 14 | a0001c0001t0001g0200 a0003c0003t0001g0003 a0003c0003t0001g0004 others(11): Show |
19 | HG01884.hp1 HG02647.hp1 HG02723.hp2 others(16): Show |
intron_variant | MODIFIER | c.1670-56G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 14/30 | chr16 | 14866499 | |||||||
| chr16:14866707 | T | G | 18 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
23 | HG01192.hp2 HG02572.hp2 HG02647.hp1 others(20): Show |
intron_variant | MODIFIER | c.1806+16T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866707 | |||||||
| chr16:14866732 | C | T | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+41C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866732 | |||||||
| chr16:14866749 | G | T | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1806+58G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866749 | |||||||
| chr16:14866790 | T | C | 22 | a0003c0003t0001g0003 a0003c0003t0001g0004 a0003c0003t0001g0011 others(19): Show |
27 | HG02145.hp1 HG02257.hp1 HG02647.hp1 others(24): Show |
intron_variant | MODIFIER | c.1806+99T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866790 | |||||||
| chr16:14866811 | C | G | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+120C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866811 | |||||||
| chr16:14866817 | G | A | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+126G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866817 | |||||||
| chr16:14866829 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1806+138C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866829 | |||||||
| chr16:14866931 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1806+240C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866931 | |||||||
| chr16:14866943 | T | C | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1806+252T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866943 | |||||||
| chr16:14866953 | C | T | 3 | a0004c0004t0001g0256 a0004c0004t0003g0020 a0004c0004t0003g0021 |
3 | HG02647.hp1 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1806+262C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866953 | |||||||
| chr16:14866992 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1806+301T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14866992 | |||||||
| chr16:14867003 | G | A | 4 | a0001c0001t0002g0205 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG01261.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+312G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867003 | |||||||
| chr16:14867065 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1806+374G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867065 | |||||||
| chr16:14867094 | A | G | 9 | a0002c0002t0001g0139 a0004c0004t0001g0132 a0004c0004t0001g0133 others(6): Show |
9 | HG01109.hp1 HG01255.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.1806+403A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867094 | |||||||
| chr16:14867149 | G | GAT | 3 | a0001c0001t0002g0249 a0001c0010t0001g0201 a0014c0025t0001g0266 |
3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1806+485_1806+486d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | ||||||
| chr16:14867149 | G | GATATATA others(9): Show |
1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1806+471_1806+486d others(18): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | ||||||
| chr16:14867149 | GAT | G | 12 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0098 others(9): Show |
12 | HG00280.hp2 HG00621.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1806+485_1806+486d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | ||||||
| chr16:14867149 | GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1806+477_1806+486d others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867149 | ||||||
| chr16:14867163 | TATATATA others(4): Show |
T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1806+473_1806+483d others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867163 | |||||||
| chr16:14867163 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1806+473_1806+485d others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867163 | |||||||
| chr16:14867168 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1806+477A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867168 | |||||||
| chr16:14867170 | A | T | 1 | a0001c0001t0001g0012 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1806+479A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867170 | |||||||
| chr16:14867172 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0155 a0002c0002t0004g0142 |
3 | HG03540.hp1 HG04204.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1806+481A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867172 | |||||||
| chr16:14867174 | A | ATTTT | 3 | a0001c0001t0001g0078 a0002c0002t0001g0089 a0002c0002t0001g0210 |
3 | HG03491.hp1 HG03492.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1806+484_1806+485i others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | ||||||
| chr16:14867174 | A | ATTTTT | 4 | a0002c0002t0001g0209 a0002c0005t0001g0229 a0002c0005t0001g0236 others(1): Show |
4 | HG00673.hp2 HG02040.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+484_1806+485i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | ||||||
| chr16:14867174 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1806+484_1806+485i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | ||||||
| chr16:14867174 | A | ATTTTTTT others(5): Show |
1 | a0001c0013t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1806+484_1806+485i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | ||||||
| chr16:14867174 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1806+483A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867174 | |||||||
| chr16:14867174 | A | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0155 others(7): Show |
10 | HG01346.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1806+483A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867174 | |||||||
| chr16:14867174 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0094 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1806+485_1806+496d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867174 | ||||||
| chr16:14867175 | TA | T | 3 | a0001c0001t0002g0194 a0001c0001t0002g0205 a0003c0003t0001g0102 |
3 | HG01261.hp2 HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1806+485delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867175 | |||||||
| chr16:14867176 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0041 a0006c0009t0001g0284 |
2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(23): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0009 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(35): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(30): Show |
1 | a0001c0008t0001g0109 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(42): Show |
1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(51): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0058 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(49): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0123 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(54): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(46): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0206 |
2 | NA18947.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(42): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(31): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0157 |
3 | HG00741.hp1 HG01981.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(40): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0118 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(44): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0022 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0059 a0001c0011t0001g0040 |
2 | HG01257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(38): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(30): Show |
1 | a0001c0011t0001g0039 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(41): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(42): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(35): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0008 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(38): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0265 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(41): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0034 a0001c0008t0001g0108 |
2 | HG02071.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(32): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(24): Show |
1 | a0001c0001t0007g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(33): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0122 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(36): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0119 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(37): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0012 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(37): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(39): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0008 a0006c0009t0001g0276 |
2 | HG01255.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(26): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(19): Show |
1 | a0001c0008t0001g0259 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(28): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(20): Show |
2 | a0001c0008t0001g0045 a0001c0008t0001g0046 |
2 | NA18982.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0048 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(32): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0013 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(26): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(19): Show |
1 | a0012c0016t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(28): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0053 a0001c0001t0001g0163 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(29): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(14): Show |
1 | a0005c0006t0001g0270 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(23): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(25): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0032 a0006c0009t0001g0272 |
2 | HG01074.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(21): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(7): Show |
1 | a0005c0006t0001g0271 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0150 a0005c0006t0001g0226 others(1): Show |
4 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(18): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0216 a0001c0001t0001g0240 others(1): Show |
4 | HG01123.hp1 HG01358.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1806+486_1806+487i others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(8): Show |
1 | a0005c0006t0001g0273 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(11): Show |
1 | a0004c0004t0003g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(20): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0005 a0009c0019t0001g0218 |
2 | HG01361.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0241 |
2 | HG00733.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(15): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(3): Show |
5 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0253 others(2): Show |
5 | HG00323.hp1 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0223 others(1): Show |
4 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATTT | 7 | a0002c0002t0001g0214 a0004c0004t0001g0133 a0004c0004t0001g0134 others(4): Show |
7 | HG01109.hp1 HG01952.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0255 |
3 | HG00609.hp2 HG01167.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATTT others(4): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0073 a0001c0001t0003g0087 |
3 | HG00738.hp1 HG01243.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATATTT others(5): Show |
6 | a0001c0001t0001g0075 a0001c0001t0001g0148 a0001c0001t0001g0262 others(3): Show |
6 | HG01074.hp1 HG02723.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTT | 5 | a0002c0002t0001g0230 a0002c0002t0001g0303 a0002c0002t0001g0305 others(2): Show |
6 | HG02015.hp2 HG02074.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTTTT | 7 | a0002c0002t0001g0018 a0002c0002t0001g0291 a0002c0002t0001g0292 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTTTT others(2): Show |
7 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0084 others(4): Show |
7 | HG00621.hp1 HG01346.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(11): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTTTT others(3): Show |
4 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0093 others(1): Show |
4 | HG01433.hp1 NA19012.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTTTT others(4): Show |
2 | a0001c0001t0001g0023 a0001c0001t0003g0064 |
2 | NA18968.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(13): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0071 a0006c0009t0003g0077 |
2 | HG00735.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1806+486_1806+487i others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTT | 16 | a0002c0002t0001g0092 a0002c0002t0001g0143 a0002c0002t0001g0212 others(13): Show |
16 | HG02027.hp1 HG02523.hp1 HG03688.hp1 others(13): Show |
intron_variant | MODIFIER | c.1806+510_1806+514d others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTT | 7 | a0002c0002t0001g0221 a0002c0002t0001g0231 a0002c0002t0001g0233 others(4): Show |
7 | HG02080.hp2 HG03927.hp2 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+509_1806+514d others(8): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTTT | 6 | a0002c0002t0001g0018 a0002c0002t0001g0211 a0002c0002t0001g0252 others(3): Show |
6 | HG00597.hp1 NA18612.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+508_1806+514d others(9): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0065 others(5): Show |
8 | HG00642.hp1 HG01123.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+506_1806+514d others(11): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | NA18960.hp1 NA18973.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+505_1806+514d others(12): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTTT others(5): Show |
1 | a0001c0013t0001g0238 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1806+503_1806+514d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1806+501_1806+514d others(16): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | A | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0028 others(29): Show |
33 | HG00621.hp2 HG00673.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1806+485A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867176 | |||||||
| chr16:14867176 | AT | A | 12 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0115 others(9): Show |
12 | HG02145.hp1 HG02572.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+514delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | ATT | A | 13 | a0001c0001t0001g0183 a0001c0001t0002g0015 a0001c0001t0002g0162 others(10): Show |
13 | HG00323.hp2 HG01258.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1806+513_1806+514d others(4): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867176 | ATTTT | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0016 others(9): Show |
18 | HG00438.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1806+511_1806+514d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867176 | ||||||
| chr16:14867177 | T | TA | 10 | a0001c0001t0001g0114 a0001c0001t0002g0014 a0001c0001t0002g0158 others(7): Show |
10 | HG01496.hp1 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1806+486_1806+487i others(3): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867177 | |||||||
| chr16:14867177 | T | TATATATA others(8): Show |
1 | a0013c0027t0001g0125 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1806+486_1806+487i others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867177 | |||||||
| chr16:14867178 | T | A | 6 | a0001c0001t0001g0103 a0001c0001t0001g0178 a0001c0001t0001g0216 others(3): Show |
6 | HG01952.hp2 HG01993.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+487T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867178 | |||||||
| chr16:14867179 | T | A | 12 | a0001c0001t0001g0114 a0001c0001t0002g0044 a0001c0001t0002g0144 others(9): Show |
12 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1806+488T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867179 | |||||||
| chr16:14867180 | T | A | 2 | a0001c0001t0002g0195 a0014c0025t0001g0266 |
2 | HG00323.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+489T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867180 | |||||||
| chr16:14867181 | T | A | 8 | a0001c0001t0006g0179 a0003c0003t0001g0024 a0003c0003t0001g0025 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+490T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867181 | |||||||
| chr16:14867182 | T | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0187 others(6): Show |
12 | HG00438.hp2 HG02056.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.1806+491T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867182 | |||||||
| chr16:14867183 | T | A | 7 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+492T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867183 | |||||||
| chr16:14867184 | T | A | 2 | a0001c0001t0002g0192 a0014c0025t0001g0266 |
2 | HG00438.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+493T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867184 | |||||||
| chr16:14867185 | T | A | 7 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1806+494T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867185 | |||||||
| chr16:14867186 | T | A | 2 | a0001c0001t0002g0192 a0014c0025t0001g0266 |
2 | HG00438.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1806+495T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867186 | |||||||
| chr16:14867187 | T | A | 6 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1806+496T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867187 | |||||||
| chr16:14867189 | T | A | 2 | a0003c0003t0001g0025 a0008c0012t0001g0126 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1806+498T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867189 | |||||||
| chr16:14867230 | C | T | 1 | a0006c0009t0003g0077 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1806+539C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867230 | |||||||
| chr16:14867248 | T | C | 5 | a0003c0003t0001g0102 a0008c0012t0001g0126 a0008c0012t0001g0127 others(2): Show |
5 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1806+557T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867248 | |||||||
| chr16:14867311 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1806+620C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867311 | |||||||
| chr16:14867324 | A | G | 8 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1806+633A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867324 | |||||||
| chr16:14867333 | G | A | 2 | a0002c0002t0001g0297 a0002c0002t0001g0300 |
2 | HG02080.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1806+642G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867333 | |||||||
| chr16:14867347 | C | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0032 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.1806+656C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867347 | |||||||
| chr16:14867481 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(225): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1806+790T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867481 | |||||||
| chr16:14867524 | T | C | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1806+833T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867524 | |||||||
| chr16:14867620 | C | T | 2 | a0001c0001t0002g0161 a0014c0025t0001g0266 |
2 | HG03139.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1807-928C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867620 | |||||||
| chr16:14867644 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0114 others(11): Show |
20 | HG01993.hp2 HG02486.hp2 HG03490.hp2 others(17): Show |
intron_variant | MODIFIER | c.1807-904A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867644 | |||||||
| chr16:14867679 | C | T | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-869C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867679 | |||||||
| chr16:14867774 | C | T | 2 | a0001c0013t0001g0146 a0001c0013t0001g0238 |
2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1807-774C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867774 | |||||||
| chr16:14867775 | G | C | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-773G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867775 | |||||||
| chr16:14867812 | G | A | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1807-736G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14867812 | |||||||
| chr16:14867894 | C | CT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0022 others(23): Show |
29 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1807-638dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 14867894 | ||||||
| chr16:14868033 | T | C | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1807-515T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868033 | |||||||
| chr16:14868058 | T | A | 1 | a0001c0001t0002g0006 | 3 | NA18948.hp1 NA18994.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1807-490T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868058 | |||||||
| chr16:14868103 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(305): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1807-445T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868103 | |||||||
| chr16:14868441 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(46): Show |
53 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1807-107A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868441 | |||||||
| chr16:14868449 | T | C | 1 | a0003c0003t0001g0011 | 2 | NA19062.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1807-99T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868449 | |||||||
| chr16:14868508 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1807-40A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868508 | |||||||
| chr16:14868541 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1807-7T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 15/30 | chr16 | 14868541 | |||||||
| chr16:14868682 | G | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG01192.hp2 NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1894+47G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868682 | |||||||
| chr16:14868909 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1894+274T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868909 | |||||||
| chr16:14868978 | A | G | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+343A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14868978 | |||||||
| chr16:14869001 | T | C | 1 | a0005c0006t0001g0271 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1894+366T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869001 | |||||||
| chr16:14869185 | G | A | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+550G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869185 | |||||||
| chr16:14869223 | C | T | 1 | a0006c0009t0001g0284 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1894+588C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869223 | |||||||
| chr16:14869340 | A | G | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1894+705A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869340 | |||||||
| chr16:14869353 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
73 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1894+718T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869353 | |||||||
| chr16:14869411 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894+776G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869411 | |||||||
| chr16:14869707 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1894+1072C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869707 | |||||||
| chr16:14869843 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(242): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1894+1208G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869843 | |||||||
| chr16:14869854 | C | A | 1 | a0007c0007t0001g0287 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1894+1219C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869854 | |||||||
| chr16:14869935 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1894+1300G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14869935 | |||||||
| chr16:14870074 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(203): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1894+1439C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870074 | |||||||
| chr16:14870265 | G | T | 3 | a0002c0002t0004g0141 a0002c0002t0004g0142 a0002c0002t0004g0239 |
3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1895-1356G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870265 | |||||||
| chr16:14870386 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0104 |
2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1895-1235T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870386 | |||||||
| chr16:14870434 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1895-1187C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870434 | |||||||
| chr16:14870623 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1895-998G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870623 | |||||||
| chr16:14870653 | C | G | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1895-968C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870653 | |||||||
| chr16:14870711 | A | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(40): Show |
46 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.1895-910A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870711 | |||||||
| chr16:14870711 | A | G | 1 | a0002c0002t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1895-910A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870711 | |||||||
| chr16:14870717 | A | G | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1895-904A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870717 | |||||||
| chr16:14870887 | C | T | 5 | a0001c0001t0003g0064 a0001c0001t0003g0087 a0001c0001t0003g0117 others(2): Show |
5 | NA18957.hp1 NA18961.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1895-734C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14870887 | |||||||
| chr16:14871139 | G | C | 1 | a0004c0004t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1895-482G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871139 | |||||||
| chr16:14871140 | C | T | 1 | a0004c0004t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1895-481C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871140 | |||||||
| chr16:14871383 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1895-238A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871383 | |||||||
| chr16:14871403 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1895-218G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871403 | |||||||
| chr16:14871434 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1895-187T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871434 | |||||||
| chr16:14871467 | G | A | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1895-154G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871467 | |||||||
| chr16:14871576 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1895-45A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 16/30 | chr16 | 14871576 | |||||||
| chr16:14871729 | G | A | 1 | a0010c0023t0002g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1958+45G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14871729 | |||||||
| chr16:14871969 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1959-265G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14871969 | |||||||
| chr16:14872123 | G | A | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1959-111G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 17/30 | chr16 | 14872123 | |||||||
| chr16:14872835 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2054+506G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872835 | |||||||
| chr16:14872875 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2054+546C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872875 | |||||||
| chr16:14872919 | T | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0032 others(30): Show |
36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.2054+590T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14872919 | |||||||
| chr16:14873006 | C | T | 8 | a0005c0006t0001g0226 a0005c0006t0001g0270 a0005c0006t0001g0271 others(5): Show |
8 | HG00140.hp2 HG01074.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.2054+677C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873006 | |||||||
| chr16:14873007 | G | A | 67 | a0002c0002t0001g0018 a0002c0002t0001g0089 a0002c0002t0001g0092 others(64): Show |
69 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.2054+678G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873007 | |||||||
| chr16:14873151 | T | TA | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(165): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.2054+825dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14873151 | ||||||
| chr16:14873302 | GA | G | 65 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0028 others(62): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.2054+976delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14873302 | ||||||
| chr16:14873439 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2054+1110G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873439 | |||||||
| chr16:14873564 | C | T | 9 | a0001c0001t0001g0079 a0001c0010t0001g0160 a0002c0005t0001g0091 others(6): Show |
9 | HG00673.hp2 HG06807.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.2054+1235C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873564 | |||||||
| chr16:14873565 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2054+1236G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873565 | |||||||
| chr16:14873670 | A | G | 20 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
21 | HG01255.hp1 HG02027.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2054+1341A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873670 | |||||||
| chr16:14873799 | G | A | 6 | a0001c0013t0001g0238 a0001c0020t0002g0175 a0003c0003t0001g0024 others(3): Show |
6 | HG01106.hp2 HG02257.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.2055-1237G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873799 | |||||||
| chr16:14873803 | T | G | 8 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0013t0001g0238 others(5): Show |
8 | HG01106.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2055-1233T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873803 | |||||||
| chr16:14873824 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(42): Show |
48 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.2055-1212C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873824 | |||||||
| chr16:14873972 | A | G | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2055-1064A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873972 | |||||||
| chr16:14873986 | G | A | 2 | a0001c0001t0002g0207 a0002c0002t0001g0257 |
2 | NA18997.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2055-1050G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14873986 | |||||||
| chr16:14874022 | TTGGTCTG others(69): Show |
T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(157): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.2055-986_2055-911d others(78): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 14874022 | ||||||
| chr16:14874098 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2055-938C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874098 | |||||||
| chr16:14874119 | G | A | 8 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0246 others(5): Show |
8 | HG02145.hp1 HG02895.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055-917G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874119 | |||||||
| chr16:14874136 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | NA18960.hp1 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2055-900C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874136 | |||||||
| chr16:14874141 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2055-895T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874141 | |||||||
| chr16:14874144 | C | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0100 others(25): Show |
34 | HG01109.hp2 HG01993.hp2 HG02145.hp1 others(31): Show |
intron_variant | MODIFIER | c.2055-892C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874144 | |||||||
| chr16:14874185 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0016 a0001c0001t0002g0187 others(2): Show |
8 | HG00438.hp2 HG02056.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2055-851G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874185 | |||||||
| chr16:14874625 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2055-411A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874625 | |||||||
| chr16:14874925 | T | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0100 others(21): Show |
30 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.2055-111T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14874925 | |||||||
| chr16:14875002 | C | T | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(43): Show |
49 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.2055-34C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875002 | |||||||
| chr16:14875021 | C | T | 1 | a0010c0023t0002g0199 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2055-15C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875021 | |||||||
| chr16:14875023 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2055-13G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 18/30 | chr16 | 14875023 | |||||||
| chr16:14875271 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2273+17G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 19/30 | chr16 | 14875271 | |||||||
| chr16:14875569 | TTGGATGG others(5): Show |
T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0032 others(16): Show |
22 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(19): Show |
intron_variant | MODIFIER | c.2356+163_2356+174d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875569 | ||||||
| chr16:14875602 | T | TTGGA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0084 a0001c0001t0001g0095 others(11): Show |
14 | HG00621.hp1 HG01884.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.2356+219_2356+222d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | ||||||
| chr16:14875602 | TTGGA | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
59 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.2356+219_2356+222d others(6): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | ||||||
| chr16:14875602 | TTGGATGG others(13): Show |
T | 1 | a0001c0014t0001g0113 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2356+203_2356+222d others(22): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 14875602 | ||||||
| chr16:14875645 | A | G | 1 | a0002c0002t0001g0305 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2356+223A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875645 | |||||||
| chr16:14875892 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0183 |
2 | HG01258.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2357-467T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875892 | |||||||
| chr16:14875937 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2357-422T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14875937 | |||||||
| chr16:14876067 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2357-292C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876067 | |||||||
| chr16:14876104 | C | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(220): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2357-255C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876104 | |||||||
| chr16:14876180 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2357-179G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876180 | |||||||
| chr16:14876206 | C | T | 1 | a0002c0005t0001g0236 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2357-153C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876206 | |||||||
| chr16:14876333 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2357-26C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 20/30 | chr16 | 14876333 | |||||||
| chr16:14876542 | G | T | 1 | a0001c0010t0001g0201 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2516+24G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 21/30 | chr16 | 14876542 | |||||||
| chr16:14876817 | C | G | 3 | a0002c0002t0004g0141 a0002c0002t0004g0142 a0002c0002t0004g0239 |
3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2643+27C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14876817 | |||||||
| chr16:14876953 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(227): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2643+163T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14876953 | |||||||
| chr16:14877012 | C | T | 1 | a0001c0020t0002g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2643+222C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877012 | |||||||
| chr16:14877155 | G | GT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(53): Show |
60 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.2643+381dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14877155 | ||||||
| chr16:14877158 | T | G | 4 | a0001c0001t0002g0268 a0004c0004t0001g0256 a0004c0004t0003g0020 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2643+368T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877158 | |||||||
| chr16:14877506 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2643+716C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877506 | |||||||
| chr16:14877625 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2643+835G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877625 | |||||||
| chr16:14877626 | C | G | 1 | a0002c0002t0001g0303 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2643+836C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877626 | |||||||
| chr16:14877738 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2643+948G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877738 | |||||||
| chr16:14877809 | G | GTGGTTAC others(8): Show |
1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-908_2644-894d others(17): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14877809 | ||||||
| chr16:14877888 | A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-833A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877888 | |||||||
| chr16:14877891 | A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-830A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877891 | |||||||
| chr16:14877892 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-829A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877892 | |||||||
| chr16:14877893 | T | A | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-828T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877893 | |||||||
| chr16:14877911 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-810A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877911 | |||||||
| chr16:14877915 | T | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-806T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877915 | |||||||
| chr16:14877915 | T | TAAAAC | 305 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(302): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.2644-806_2644-805i others(7): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877915 | |||||||
| chr16:14877935 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2644-786A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877935 | |||||||
| chr16:14877950 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-771A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14877950 | |||||||
| chr16:14878086 | A | T | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2644-635A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878086 | |||||||
| chr16:14878271 | A | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG01243.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2644-450A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878271 | |||||||
| chr16:14878404 | G | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-317G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878404 | |||||||
| chr16:14878407 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-314T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878407 | |||||||
| chr16:14878493 | C | CA | 32 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0057 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.2644-200dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | ||||||
| chr16:14878493 | CA | C | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(27): Show |
30 | HG00438.hp2 HG01109.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.2644-200delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | ||||||
| chr16:14878493 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2644-211_2644-200d others(14): Show |
NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | 14878493 | ||||||
| chr16:14878516 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-205A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878516 | |||||||
| chr16:14878517 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-204A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878517 | |||||||
| chr16:14878638 | A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-83A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878638 | |||||||
| chr16:14878668 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2644-53T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 22/30 | chr16 | 14878668 | |||||||
| chr16:14878899 | G | A | 3 | a0001c0008t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0259 |
3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2757+65G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878899 | |||||||
| chr16:14878907 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+73C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878907 | |||||||
| chr16:14878916 | T | A | 1 | a0002c0002t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2757+82T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878916 | |||||||
| chr16:14878923 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2757+89G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878923 | |||||||
| chr16:14878935 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+101A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14878935 | |||||||
| chr16:14879019 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2757+185T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879019 | |||||||
| chr16:14879033 | C | A | 1 | a0002c0002t0001g0297 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2757+199C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879033 | |||||||
| chr16:14879058 | A | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(3): Show |
6 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2757+224A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879058 | |||||||
| chr16:14879060 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2757+226T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879060 | |||||||
| chr16:14879116 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(4): Show |
7 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.2757+282A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879116 | |||||||
| chr16:14879123 | C | T | 1 | a0004c0004t0001g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2757+289C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879123 | |||||||
| chr16:14879134 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(2): Show |
5 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2757+300G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879134 | |||||||
| chr16:14879143 | C | T | 9 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 others(6): Show |
11 | HG01243.hp1 HG02717.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.2757+309C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879143 | |||||||
| chr16:14879310 | C | A | 1 | a0001c0010t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2757+476C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879310 | |||||||
| chr16:14879347 | C | T | 3 | a0001c0001t0001g0152 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG03669.hp1 HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2757+513C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879347 | |||||||
| chr16:14879503 | C | T | 2 | a0001c0001t0005g0129 a0001c0001t0005g0130 |
2 | HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2758-512C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879503 | |||||||
| chr16:14879588 | T | A | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-427T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879588 | |||||||
| chr16:14879589 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-426A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879589 | |||||||
| chr16:14879659 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-356T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879659 | |||||||
| chr16:14879740 | GA | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0220 a0001c0001t0001g0310 others(3): Show |
6 | HG00323.hp1 HG02735.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.2758-257delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr16 | 14879740 | ||||||
| chr16:14879767 | A | C | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2758-248A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879767 | |||||||
| chr16:14879893 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2758-122C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14879893 | |||||||
| chr16:14880012 | T | C | 3 | a0001c0001t0005g0129 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG03669.hp1 HG03710.hp2 NA18999.hp2 |
splice_region_variant&intron_variant | LOW | c.2758-3T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 23/30 | chr16 | 14880012 | |||||||
| chr16:14880398 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+256T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880398 | |||||||
| chr16:14880405 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+263T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880405 | |||||||
| chr16:14880416 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+274G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880416 | |||||||
| chr16:14880484 | T | C | 13 | a0001c0001t0001g0124 a0001c0020t0002g0175 a0002c0018t0001g0289 others(10): Show |
13 | HG02145.hp1 HG02257.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.2885+342T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880484 | |||||||
| chr16:14880484 | T | G | 4 | a0001c0001t0003g0064 a0001c0001t0003g0087 a0001c0001t0003g0117 others(1): Show |
4 | NA18961.hp1 NA18968.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2885+342T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880484 | |||||||
| chr16:14880671 | C | T | 9 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(6): Show |
9 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2885+529C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880671 | |||||||
| chr16:14880718 | A | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+576A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880718 | |||||||
| chr16:14880721 | T | C | 3 | a0001c0010t0001g0201 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG03579.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2885+579T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880721 | |||||||
| chr16:14880734 | A | T | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2885+592A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880734 | |||||||
| chr16:14880807 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2885+665C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880807 | |||||||
| chr16:14880903 | G | T | 1 | a0001c0013t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2886-641G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14880903 | |||||||
| chr16:14881013 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0164 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2886-531G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881013 | |||||||
| chr16:14881147 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2886-397T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881147 | |||||||
| chr16:14881173 | G | C | 3 | a0001c0008t0001g0045 a0001c0008t0001g0046 a0001c0008t0001g0259 |
3 | NA18982.hp1 NA19062.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2886-371G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881173 | |||||||
| chr16:14881213 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-331G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881213 | |||||||
| chr16:14881259 | T | G | 1 | a0001c0021t0003g0088 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2886-285T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881259 | |||||||
| chr16:14881324 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2886-220C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881324 | |||||||
| chr16:14881381 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2886-163G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881381 | |||||||
| chr16:14881392 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-152G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881392 | |||||||
| chr16:14881410 | T | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-134T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881410 | |||||||
| chr16:14881435 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(204): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2886-109A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881435 | |||||||
| chr16:14881439 | A | C | 3 | a0001c0020t0002g0175 a0002c0018t0001g0289 a0004c0004t0001g0256 |
3 | HG03453.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2886-105A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881439 | |||||||
| chr16:14881439 | A | G | 1 | a0006c0009t0001g0284 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2886-105A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881439 | |||||||
| chr16:14881504 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0080 |
2 | HG01192.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.2886-40C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881504 | |||||||
| chr16:14881505 | A | G | 1 | a0002c0002t0001g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2886-39A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 24/30 | chr16 | 14881505 | |||||||
| chr16:14881701 | G | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3027+16G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881701 | |||||||
| chr16:14881934 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3027+249G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881934 | |||||||
| chr16:14881974 | A | G | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3027+289A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14881974 | |||||||
| chr16:14882025 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(40): Show |
46 | HG00597.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.3027+340T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882025 | |||||||
| chr16:14882282 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(241): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.3028-312A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882282 | |||||||
| chr16:14882370 | G | A | 1 | a0004c0004t0001g0159 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3028-224G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882370 | |||||||
| chr16:14882570 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3028-24G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 25/30 | chr16 | 14882570 | |||||||
| chr16:14882684 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.3111+7C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882684 | |||||||
| chr16:14882725 | G | A | 3 | a0001c0001t0001g0043 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG00733.hp2 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+48G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882725 | |||||||
| chr16:14882731 | A | C | 5 | a0001c0001t0002g0044 a0001c0001t0002g0181 a0001c0001t0002g0185 others(2): Show |
5 | NA18962.hp2 NA18985.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3111+54A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882731 | |||||||
| chr16:14882781 | A | G | 1 | a0002c0002t0001g0235 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3111+104A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882781 | |||||||
| chr16:14882833 | C | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+156C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882833 | |||||||
| chr16:14882852 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+175A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882852 | |||||||
| chr16:14882888 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3111+211T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882888 | |||||||
| chr16:14882909 | C | T | 1 | a0004c0004t0001g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3111+232C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882909 | |||||||
| chr16:14882945 | A | G | 6 | a0001c0010t0001g0019 a0001c0010t0001g0160 a0001c0010t0001g0201 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3111+268A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882945 | |||||||
| chr16:14882998 | A | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+321A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14882998 | |||||||
| chr16:14883231 | T | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+554T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883231 | |||||||
| chr16:14883333 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+656C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883333 | |||||||
| chr16:14883339 | CT | C | 6 | a0001c0001t0001g0096 a0001c0001t0008g0189 a0001c0020t0002g0175 others(3): Show |
6 | HG03669.hp1 HG03704.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.3111+677delT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr16 | 14883339 | ||||||
| chr16:14883359 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+682C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883359 | |||||||
| chr16:14883478 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+801C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883478 | |||||||
| chr16:14883494 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3111+817G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883494 | |||||||
| chr16:14883521 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3111+844G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883521 | |||||||
| chr16:14883565 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3112-807C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883565 | |||||||
| chr16:14883626 | T | C | 10 | a0001c0020t0002g0175 a0002c0018t0001g0289 a0003c0003t0001g0024 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.3112-746T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14883626 | |||||||
| chr16:14884026 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-346C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884026 | |||||||
| chr16:14884145 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3112-227G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884145 | |||||||
| chr16:14884168 | C | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0173 |
2 | HG02129.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.3112-204C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884168 | |||||||
| chr16:14884212 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-160A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884212 | |||||||
| chr16:14884252 | C | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3112-120C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884252 | |||||||
| chr16:14884292 | C | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0015t0001g0254 |
3 | HG01074.hp1 HG01167.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3112-80C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884292 | |||||||
| chr16:14884350 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(246): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.3112-22T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 26/30 | chr16 | 14884350 | |||||||
| chr16:14884556 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3222+74G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884556 | |||||||
| chr16:14884558 | G | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+76G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884558 | |||||||
| chr16:14884608 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+126C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884608 | |||||||
| chr16:14884759 | C | T | 3 | a0007c0007t0001g0017 a0007c0007t0001g0287 a0007c0007t0001g0288 |
4 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3222+277C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884759 | |||||||
| chr16:14884771 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3222+289C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884771 | |||||||
| chr16:14884776 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3222+294C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884776 | |||||||
| chr16:14884806 | T | C | 6 | a0001c0020t0002g0175 a0002c0018t0001g0289 a0003c0003t0001g0004 others(3): Show |
8 | HG03669.hp1 NA18973.hp2 NA18995.hp1 others(5): Show |
intron_variant | MODIFIER | c.3222+324T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884806 | |||||||
| chr16:14884861 | T | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+379T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884861 | |||||||
| chr16:14884942 | G | T | 1 | a0012c0016t0001g0264 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3222+460G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884942 | |||||||
| chr16:14884963 | T | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+481T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884963 | |||||||
| chr16:14884996 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0065 others(7): Show |
13 | HG00735.hp2 HG01123.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.3222+514A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14884996 | |||||||
| chr16:14885105 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+623G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885105 | |||||||
| chr16:14885166 | C | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+684C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885166 | |||||||
| chr16:14885169 | C | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+687C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885169 | |||||||
| chr16:14885189 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3222+707G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885189 | |||||||
| chr16:14885281 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3222+799G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885281 | |||||||
| chr16:14885365 | CA | C | 4 | a0001c0001t0002g0177 a0001c0001t0002g0184 a0001c0001t0002g0188 others(1): Show |
4 | HG00733.hp1 HG02735.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.3222+887delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr16 | 14885365 | ||||||
| chr16:14885476 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+994A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885476 | |||||||
| chr16:14885519 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+1037A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885519 | |||||||
| chr16:14885591 | T | C | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3222+1109T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885591 | |||||||
| chr16:14885632 | A | T | 1 | a0002c0002t0001g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3223-1129A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885632 | |||||||
| chr16:14885663 | G | T | 1 | a0006c0009t0001g0284 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3223-1098G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885663 | |||||||
| chr16:14885700 | T | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-1061T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885700 | |||||||
| chr16:14885707 | G | A | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-1054G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885707 | |||||||
| chr16:14885811 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3223-950C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885811 | |||||||
| chr16:14885827 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3223-934T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885827 | |||||||
| chr16:14885976 | T | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-785T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14885976 | |||||||
| chr16:14886111 | G | C | 3 | a0001c0001t0001g0200 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG01884.hp1 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-650G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886111 | |||||||
| chr16:14886136 | G | C | 3 | a0001c0001t0001g0200 a0001c0020t0002g0175 a0002c0018t0001g0289 |
3 | HG01884.hp1 HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-625G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886136 | |||||||
| chr16:14886438 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(46): Show |
53 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.3223-323G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886438 | |||||||
| chr16:14886669 | C | T | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-92C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886669 | |||||||
| chr16:14886677 | A | G | 2 | a0001c0020t0002g0175 a0002c0018t0001g0289 |
2 | HG03669.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3223-84A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 27/30 | chr16 | 14886677 | |||||||
| chr16:14886894 | C | T | 2 | a0001c0001t0003g0117 a0001c0021t0003g0088 |
2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.3324+32C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14886894 | |||||||
| chr16:14886974 | A | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+112A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14886974 | |||||||
| chr16:14887118 | T | C | 2 | a0008c0012t0001g0126 a0008c0012t0001g0127 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3324+256T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887118 | |||||||
| chr16:14887244 | G | A | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+382G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887244 | |||||||
| chr16:14887320 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0275 |
2 | HG01123.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.3324+458G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887320 | |||||||
| chr16:14887442 | T | C | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+580T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887442 | |||||||
| chr16:14887463 | C | T | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+601C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887463 | |||||||
| chr16:14887472 | T | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+610T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887472 | |||||||
| chr16:14887474 | T | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+612T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887474 | |||||||
| chr16:14887490 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3324+628C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887490 | |||||||
| chr16:14887653 | C | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+791C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887653 | |||||||
| chr16:14887805 | A | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3324+943A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14887805 | |||||||
| chr16:14888018 | C | T | 2 | a0001c0001t0002g0181 a0001c0001t0002g0191 |
2 | NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3325-1078C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888018 | |||||||
| chr16:14888243 | A | G | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-853A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888243 | |||||||
| chr16:14888265 | C | T | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3325-831C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888265 | |||||||
| chr16:14888319 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3325-777C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888319 | |||||||
| chr16:14888398 | G | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0196 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3325-698G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888398 | |||||||
| chr16:14888425 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3325-671T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888425 | |||||||
| chr16:14888571 | T | C | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-525T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888571 | |||||||
| chr16:14888575 | T | C | 1 | a0002c0018t0001g0289 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3325-521T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888575 | |||||||
| chr16:14888609 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0034 others(6): Show |
10 | HG02027.hp2 HG02040.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.3325-487C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888609 | |||||||
| chr16:14888614 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3325-482C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888614 | |||||||
| chr16:14888703 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3325-393G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888703 | |||||||
| chr16:14888723 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(159): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.3325-373G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888723 | |||||||
| chr16:14888812 | G | A | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3325-284G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888812 | |||||||
| chr16:14888901 | A | G | 1 | a0001c0011t0002g0180 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3325-195A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888901 | |||||||
| chr16:14888944 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3325-152T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14888944 | |||||||
| chr16:14889065 | G | A | 1 | a0001c0010t0001g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3325-31G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14889065 | |||||||
| chr16:14889093 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18993.hp1 | splice_region_variant&intron_variant | LOW | c.3325-3C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 28/30 | chr16 | 14889093 | |||||||
| chr16:14889248 | T | C | 1 | a0001c0001t0002g0249 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3444+33T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889248 | |||||||
| chr16:14889276 | A | T | 1 | a0003c0003t0001g0128 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3444+61A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889276 | |||||||
| chr16:14889311 | C | G | 73 | a0002c0002t0001g0018 a0002c0002t0001g0089 a0002c0002t0001g0092 others(70): Show |
75 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.3444+96C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889311 | |||||||
| chr16:14889322 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3444+107A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889322 | |||||||
| chr16:14889562 | C | A | 2 | a0001c0001t0002g0279 a0001c0001t0006g0179 |
2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3444+347C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889562 | |||||||
| chr16:14889582 | G | A | 1 | a0001c0001t0006g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3444+367G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889582 | |||||||
| chr16:14889616 | A | G | 24 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0100 others(21): Show |
30 | HG01109.hp2 HG01993.hp2 HG02451.hp2 others(27): Show |
intron_variant | MODIFIER | c.3444+401A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889616 | |||||||
| chr16:14889861 | A | G | 1 | a0006c0009t0001g0284 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3444+646A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14889861 | |||||||
| chr16:14890104 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3444+889A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890104 | |||||||
| chr16:14890110 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0023 others(45): Show |
52 | HG00609.hp2 HG00621.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.3444+895G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890110 | |||||||
| chr16:14890321 | C | T | 1 | a0001c0010t0001g0019 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3444+1106C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890321 | |||||||
| chr16:14890667 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(220): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.3444+1452G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890667 | |||||||
| chr16:14890988 | T | C | 3 | a0002c0002t0004g0141 a0002c0002t0004g0142 a0002c0002t0004g0239 |
3 | HG02145.hp2 HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3444+1773T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14890988 | |||||||
| chr16:14891057 | G | A | 1 | a0004c0004t0001g0134 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3444+1842G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891057 | |||||||
| chr16:14891120 | G | A | 1 | a0018c0026t0001g0311 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3444+1905G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891120 | |||||||
| chr16:14891212 | G | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG03834.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3444+1997G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891212 | |||||||
| chr16:14891437 | T | G | 1 | a0002c0002t0001g0303 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3444+2222T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891437 | |||||||
| chr16:14891904 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3444+2689A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891904 | |||||||
| chr16:14891952 | C | T | 2 | a0001c0001t0001g0114 a0002c0005t0001g0227 |
2 | HG02486.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.3444+2737C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14891952 | |||||||
| chr16:14892223 | C | T | 1 | a0002c0002t0001g0301 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3445-2775C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892223 | |||||||
| chr16:14892242 | C | CA | 6 | a0001c0001t0003g0064 a0001c0001t0003g0087 a0001c0001t0003g0117 others(3): Show |
6 | HG01257.hp1 HG01258.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3445-2744dupA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14892242 | ||||||
| chr16:14892253 | A | G | 8 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3445-2745A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892253 | |||||||
| chr16:14892328 | T | C | 3 | a0007c0007t0001g0017 a0007c0007t0001g0287 a0007c0007t0001g0288 |
4 | NA18947.hp2 NA18962.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.3445-2670T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892328 | |||||||
| chr16:14892351 | G | A | 1 | a0002c0005t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3445-2647G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892351 | |||||||
| chr16:14892609 | TA | T | 18 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(15): Show |
18 | HG00140.hp1 HG01257.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3445-2370delA | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14892609 | ||||||
| chr16:14892683 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3445-2315A>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892683 | |||||||
| chr16:14892686 | G | A | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3445-2312G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892686 | |||||||
| chr16:14892836 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3445-2162G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892836 | |||||||
| chr16:14892898 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(216): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.3445-2100T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892898 | |||||||
| chr16:14892904 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(217): Show |
232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.3445-2094C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892904 | |||||||
| chr16:14892912 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3445-2086G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14892912 | |||||||
| chr16:14893156 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3445-1842T>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893156 | |||||||
| chr16:14893161 | C | CT | 3 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0059 |
3 | HG01243.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3445-1836dupT | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | INFO_REALIGN_3_PRIME | chr16 | 14893161 | ||||||
| chr16:14893284 | T | C | 2 | a0008c0012t0001g0126 a0008c0012t0001g0127 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3445-1714T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893284 | |||||||
| chr16:14893289 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3445-1709G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893289 | |||||||
| chr16:14893552 | A | G | 1 | a0001c0001t0007g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3445-1446A>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893552 | |||||||
| chr16:14893638 | G | C | 9 | a0001c0008t0001g0108 a0003c0003t0001g0024 a0003c0003t0001g0025 others(6): Show |
9 | HG02071.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3445-1360G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893638 | |||||||
| chr16:14893669 | C | T | 3 | a0008c0012t0001g0126 a0008c0012t0001g0127 a0013c0027t0001g0125 |
3 | HG02145.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3445-1329C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893669 | |||||||
| chr16:14893923 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0007g0260 |
2 | HG01433.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3445-1075C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14893923 | |||||||
| chr16:14894024 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3445-974T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894024 | |||||||
| chr16:14894064 | G | A | 1 | a0002c0002t0001g0283 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3445-934G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894064 | |||||||
| chr16:14894096 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3445-902A>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894096 | |||||||
| chr16:14894324 | C | A | 1 | a0002c0002t0001g0234 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3445-674C>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894324 | |||||||
| chr16:14894391 | C | G | 4 | a0003c0003t0001g0004 a0003c0003t0001g0105 a0003c0003t0001g0106 others(1): Show |
6 | NA18973.hp2 NA18995.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.3445-607C>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894391 | |||||||
| chr16:14894413 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3445-585G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894413 | |||||||
| chr16:14894414 | G | A | 1 | a0014c0025t0001g0266 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3445-584G>A | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894414 | |||||||
| chr16:14894441 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3445-557C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894441 | |||||||
| chr16:14894511 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3445-487G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894511 | |||||||
| chr16:14894824 | T | C | 1 | a0001c0001t0008g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3445-174T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894824 | |||||||
| chr16:14894837 | T | C | 4 | a0002c0002t0001g0092 a0002c0002t0001g0231 a0002c0002t0001g0235 others(1): Show |
4 | NA18985.hp1 NA19004.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.3445-161T>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894837 | |||||||
| chr16:14894948 | G | C | 1 | a0003c0003t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3445-50G>C | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894948 | |||||||
| chr16:14894953 | T | G | 3 | a0001c0001t0008g0189 a0002c0005t0001g0227 a0002c0005t0001g0244 |
3 | HG03704.hp2 NA18963.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3445-45T>G | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894953 | |||||||
| chr16:14894955 | G | T | 3 | a0001c0001t0008g0189 a0002c0005t0001g0227 a0002c0005t0001g0244 |
3 | HG03704.hp2 NA18963.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.3445-43G>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 29/30 | chr16 | 14894955 | |||||||
| chr16:14895108 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG00741.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.3537+18C>T | NOMO1 | ENSG00000103512.16 | transcript | ENST00000287667.12 | protein_coding | 30/30 | chr16 | 14895108 |