Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51203 |
| ensemblid | ENSG00000137804.14 |
| hgncid | 18538 |
| symbol | NUSAP1 |
| name | nucleolar and spindle associated protein 1 |
| refseq_nuc | NM_016359.5 |
| refseq_prot | NP_057443.2 |
| ensembl_nuc | ENST00000559596.6 |
| ensembl_prot | ENSP00000453403.1 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 41332881 |
| end | 41381046 |
| strand | + |
| ver | v1.2 |
| region | chr15:41332881-41381046 |
| region5000 | chr15:41327881-41386046 |
| regionname0 | NUSAP1_chr15_41332881_41381046 |
| regionname5000 | NUSAP1_chr15_41327881_41386046 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 441 | 175 | 32 | 32 | 71 | 6 | 32 | 51 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | MIIPS others(436): Show |
chr15 | 41327881 | 41386046 |
| a0002 | 0/0 | 441 | 110 | 44 | 22 | 24 | 8 | 12 | 20 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | MIIPS others(436): Show |
chr15 | 41327881 | 41386046 |
| a0003 | 0/0 | 441 | 6 | 4 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | MIIPS others(436): Show |
chr15 | 41327881 | 41386046 |
| a0004 | 0/0 | 441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | MIIPS others(436): Show |
chr15 | 41327881 | 41386046 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1323 | 175 | 32 | 32 | 71 | 6 | 32 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 | ||
| a0002c0002 | 0/0 | 1323 | 107 | 41 | 22 | 24 | 8 | 12 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 | ||
| a0002c0004 | 0/0 | 1323 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 | ||
| a0002c0005 | 0/0 | 1323 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 | ||
| a0003c0003 | 0/0 | 1323 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 | ||
| a0004c0006 | 0/0 | 1323 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | ATGAT others(1318): Show |
chr15 | 41327881 | 41386046 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2263 | 116 | 31 | 17 | 36 | 6 | 25 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0001c0001t0002 | 0/1 | 2264 | 56 | 1 | 15 | 33 | 0 | 6 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0001c0001t0004 | 0/0 | 2263 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0001c0001t0007 | 0/0 | 2264 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGT others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0001 | 0/0 | 2263 | 59 | 26 | 8 | 23 | 1 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0002 | 0/0 | 2264 | 11 | 10 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0003 | 0/0 | 2264 | 21 | 0 | 8 | 1 | 4 | 8 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0004 | 0/0 | 2263 | 13 | 5 | 4 | 0 | 2 | 2 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0006 | 0/0 | 2264 | 2 | 0 | 0 | 0 | 1 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0002c0002t0008 | 0/0 | 2264 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2259): Show |
chr15 | 41327881 | 41386046 |
| a0002c0004t0004 | 0/0 | 2263 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0002c0005t0004 | 0/0 | 2263 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0003c0003t0005 | 0/0 | 2263 | 6 | 4 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| a0004c0006t0001 | 0/0 | 2263 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | GTGGC others(2258): Show |
chr15 | 41327881 | 41386046 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0002t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0004t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0004t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0002c0005t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0003c0003t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| a0004c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0011 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00099 | hp2 | a0002 | c0002 | t0003 | g0219 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0233 | EUR | GBR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00323 | hp2 | a0002 | c0002 | t0003 | g0203 | EUR | FIN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0226 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0209 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0222 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00741 | hp1 | a0002 | c0002 | t0003 | g0223 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01074 | hp2 | a0002 | c0002 | t0003 | g0204 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0224 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01081 | hp2 | a0002 | c0002 | t0004 | g0186 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0185 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01109 | hp1 | a0003 | c0003 | t0005 | g0180 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01243 | hp2 | a0003 | c0003 | t0005 | g0181 | AMR | PUR | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01257 | hp2 | a0002 | c0002 | t0004 | g0190 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01258 | hp1 | a0002 | c0002 | t0004 | g0009 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01358 | hp1 | a0002 | c0002 | t0003 | g0225 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01361 | hp1 | a0002 | c0002 | t0008 | g0217 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01515 | hp1 | a0002 | c0002 | t0004 | g0009 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01515 | hp2 | a0002 | c0002 | t0003 | g0228 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01517 | hp1 | a0002 | c0002 | t0004 | g0188 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0194 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01975 | hp1 | a0002 | c0002 | t0003 | g0229 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0211 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0173 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02145 | hp2 | a0003 | c0003 | t0005 | g0179 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | CDX | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CDX | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0266 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0214 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0202 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02572 | hp2 | a0002 | c0004 | t0004 | g0198 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02602 | hp1 | a0002 | c0002 | t0003 | g0218 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02615 | hp1 | a0002 | c0004 | t0004 | g0195 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02922 | hp2 | a0003 | c0003 | t0005 | g0176 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0196 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0193 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0210 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0213 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03491 | hp1 | a0002 | c0002 | t0003 | g0220 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03492 | hp2 | a0002 | c0002 | t0003 | g0221 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0276 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03710 | hp1 | a0002 | c0002 | t0006 | g0014 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0200 | SAS | PJL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0216 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03942 | hp1 | a0002 | c0002 | t0003 | g0232 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04184 | hp1 | a0002 | c0002 | t0003 | g0227 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0015 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04204 | hp2 | a0002 | c0002 | t0004 | g0192 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0231 | SAS | STU | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18906 | hp2 | a0003 | c0003 | t0005 | g0178 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18944 | hp1 | a0004 | c0006 | t0001 | g0251 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18985 | hp2 | a0001 | c0001 | t0007 | g0172 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0191 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20129 | hp2 | a0003 | c0003 | t0005 | g0177 | AFR | ASW | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20805 | hp2 | a0002 | c0002 | t0006 | g0230 | EUR | TSI | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | GIH | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | GIH | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0215 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0152 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0265 | AFR | ACB | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | MSL | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0187 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0234 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | USA | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA21309 | hp1 | a0002 | c0005 | t0004 | g0189 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | LWK | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0016 | REF | REF | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0052 | REF | REF | NUSAP1_chr15_41327881_41386046 | NUSAP1 | chr15 | 41327881 | 41386046 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41342389 | A | G | 3 | a0002 a0003 a0004 |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
missense_variant | MODERATE | c.97A>G | p.Thr33Ala | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/11 | 174/2263 | 97/1326 | 33/441 | chr15 | 41342389 | |||
| chr15:41342390 | C | A | 3 | a0002 a0003 a0004 |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
missense_variant | MODERATE | c.98C>A | p.Thr33Asn | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/11 | 175/2263 | 98/1326 | 33/441 | chr15 | 41342390 | |||
| chr15:41349234 | A | G | 1 | a0003 | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
missense_variant | MODERATE | c.299A>G | p.Asp100Gly | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/11 | 376/2263 | 299/1326 | 100/441 | chr15 | 41349234 | |||
| chr15:41365433 | C | T | 1 | a0004 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.692C>T | p.Thr231Ile | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/11 | 769/2263 | 692/1326 | 231/441 | chr15 | 41365433 | |||
| chr15:41380186 | A | G | 1 | a0002 | 24 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(21): Show |
stop_retained_variant | LOW | c.1326A>G | p.Ter442Ter | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 1403/2263 | 1326/1326 | 442/441 | chr15 | 41380186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41349124 | T | G | 1 | a0002c0005 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.189T>G | p.Ser63Ser | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/11 | 266/2263 | 189/1326 | 63/441 | chr15 | 41349124 | |||
| chr15:41375746 | G | A | 1 | a0002c0004 | 2 | HG02572.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.1041G>A | p.Thr347Thr | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/11 | 1118/2263 | 1041/1326 | 347/441 | chr15 | 41375746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41332885 | C | T | 1 | a0001c0001t0007 | 2 | HG02083.hp1 NA18985.hp2 |
5_prime_UTR_variant | MODIFIER | c.-73C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/11 | 73 | chr15 | 41332885 | ||||||
| chr15:41380243 | A | AT | 6 | a0001c0001t0002 a0001c0001t0007 a0002c0002t0002 others(3): Show |
92 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*69dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 70 | INFO_REALIGN_3_PRIME | chr15 | 41380243 | |||||
| chr15:41380382 | T | G | 1 | a0002c0002t0008 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 196 | chr15 | 41380382 | ||||||
| chr15:41380398 | T | G | 1 | a0003c0003t0005 | 6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*212T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 212 | chr15 | 41380398 | ||||||
| chr15:41380471 | T | A | 4 | a0001c0001t0004 a0002c0002t0004 a0002c0004t0004 others(1): Show |
17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*285T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 285 | chr15 | 41380471 | ||||||
| chr15:41380472 | C | A | 4 | a0001c0001t0004 a0002c0002t0004 a0002c0004t0004 others(1): Show |
17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 286 | chr15 | 41380472 | ||||||
| chr15:41380703 | A | T | 1 | a0002c0002t0006 | 2 | HG03710.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*517A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 11/11 | 517 | chr15 | 41380703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41333249 | G | A | 1 | a0002c0002t0001g0011 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.93+199G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333249 | |||||||
| chr15:41333362 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0002g0012 |
2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.93+312G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333362 | |||||||
| chr15:41333452 | A | T | 46 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0237 others(43): Show |
47 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.93+402A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333452 | |||||||
| chr15:41333530 | T | G | 1 | a0002c0002t0006g0014 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+480T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333530 | |||||||
| chr15:41333776 | A | G | 2 | a0002c0002t0001g0235 a0002c0002t0001g0236 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.93+726A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333776 | |||||||
| chr15:41333908 | T | C | 1 | a0002c0002t0004g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.93+858T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333908 | |||||||
| chr15:41333950 | A | G | 64 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0184 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+900A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41333950 | |||||||
| chr15:41334067 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.93+1017A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334067 | |||||||
| chr15:41334069 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18959.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.93+1019A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334069 | |||||||
| chr15:41334099 | AT | A | 46 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0237 others(43): Show |
47 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.93+1059delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41334099 | ||||||
| chr15:41334110 | ATTTG | A | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+1076_93+1079del others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41334110 | ||||||
| chr15:41334381 | A | G | 64 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0184 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.93+1331A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334381 | |||||||
| chr15:41334755 | C | T | 2 | a0001c0001t0007g0172 a0001c0001t0007g0173 |
2 | HG02083.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.93+1705C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334755 | |||||||
| chr15:41334799 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.93+1749C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334799 | |||||||
| chr15:41334837 | C | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.93+1787C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334837 | |||||||
| chr15:41334993 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.93+1943G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41334993 | |||||||
| chr15:41335058 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.93+2008G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335058 | |||||||
| chr15:41335272 | A | ATATT | 113 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0168 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.93+2225_93+2226ins others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41335272 | ||||||
| chr15:41335289 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.93+2239T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335289 | |||||||
| chr15:41335360 | TAAAC | T | 19 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0163 others(16): Show |
23 | HG00609.hp2 HG01109.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.93+2311_93+2314del others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335360 | |||||||
| chr15:41335482 | G | T | 16 | a0002c0002t0001g0197 a0002c0002t0004g0009 a0002c0002t0004g0015 others(13): Show |
17 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.93+2432G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335482 | |||||||
| chr15:41335527 | A | G | 2 | a0001c0001t0001g0171 a0002c0002t0002g0152 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.93+2477A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335527 | |||||||
| chr15:41335595 | A | T | 1 | a0002c0002t0001g0280 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.93+2545A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335595 | |||||||
| chr15:41335643 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.93+2593A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335643 | |||||||
| chr15:41335654 | TATATAAA others(8): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.93+2625_93+2639del others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41335654 | ||||||
| chr15:41335655 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.93+2605A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335655 | |||||||
| chr15:41335824 | A | G | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.93+2774A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41335824 | |||||||
| chr15:41336038 | T | C | 1 | a0002c0002t0006g0014 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.93+2988T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336038 | |||||||
| chr15:41336102 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.93+3052A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336102 | |||||||
| chr15:41336121 | G | A | 12 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(9): Show |
13 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.93+3071G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336121 | |||||||
| chr15:41336152 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.93+3102C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336152 | |||||||
| chr15:41336268 | A | AAAT | 7 | a0001c0001t0001g0058 a0001c0001t0002g0037 a0001c0001t0002g0091 others(4): Show |
7 | HG01081.hp1 HG01169.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.93+3245_93+3247dup others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | ||||||
| chr15:41336268 | A | AAATAAT | 13 | a0002c0002t0001g0197 a0002c0002t0004g0009 a0002c0002t0004g0185 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+3242_93+3247dup others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | ||||||
| chr15:41336268 | AAAT | A | 50 | a0001c0001t0001g0040 a0001c0001t0002g0039 a0001c0001t0002g0041 others(47): Show |
51 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.93+3245_93+3247del others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336268 | ||||||
| chr15:41336646 | T | C | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.93+3596T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336646 | |||||||
| chr15:41336648 | G | GT | 34 | a0001c0001t0001g0018 a0001c0001t0001g0129 a0001c0001t0001g0130 others(31): Show |
35 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.93+3619dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTGTTTTT others(3): Show |
3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0003g0203 |
3 | HG00323.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.93+3599_93+3600ins others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTT | 30 | a0002c0002t0001g0011 a0002c0002t0001g0168 a0002c0002t0001g0241 others(27): Show |
30 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.93+3614_93+3619dup others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT | 14 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0268 others(11): Show |
14 | HG01981.hp1 HG02004.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.93+3613_93+3619dup others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT others(5): Show |
4 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(1): Show |
4 | HG02145.hp2 HG02922.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.93+3608_93+3619dup others(12): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT others(6): Show |
2 | a0003c0003t0005g0180 a0003c0003t0005g0181 |
2 | HG01109.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.93+3607_93+3619dup others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT others(7): Show |
1 | a0002c0002t0001g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.93+3606_93+3619dup others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT others(9): Show |
1 | a0002c0002t0001g0235 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.93+3604_93+3619dup others(16): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | GTTTTTTT others(10): Show |
1 | a0002c0002t0001g0236 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.93+3603_93+3619dup others(17): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336648 | ||||||
| chr15:41336648 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.93+3598G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336648 | |||||||
| chr15:41336650 | T | G | 34 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.93+3600T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336650 | |||||||
| chr15:41336654 | T | TTTGTTTT others(13): Show |
2 | a0002c0002t0003g0232 a0002c0002t0003g0233 |
2 | HG00140.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.93+3606_93+3607ins others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336654 | ||||||
| chr15:41336655 | T | TTGTTTTT others(12): Show |
1 | a0002c0002t0003g0200 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.93+3606_93+3607ins others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336655 | ||||||
| chr15:41336655 | T | TTGTTTTT others(12): Show |
31 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(28): Show |
31 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.93+3606_93+3607ins others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336655 | ||||||
| chr15:41336659 | T | TGTTTGTT others(2): Show |
3 | a0002c0002t0002g0201 a0002c0002t0002g0202 a0002c0002t0003g0203 |
3 | HG00323.hp2 HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.93+3609_93+3610ins others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336659 | |||||||
| chr15:41336759 | ACCTCAGC others(2): Show |
A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.93+3713_93+3721del others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336759 | ||||||
| chr15:41336799 | A | G | 1 | a0002c0002t0003g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.93+3749A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336799 | |||||||
| chr15:41336811 | C | A | 1 | a0002c0002t0002g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.93+3761C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336811 | |||||||
| chr15:41336891 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93+3841C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336891 | |||||||
| chr15:41336929 | T | G | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.93+3879T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41336929 | |||||||
| chr15:41336999 | C | CT | 21 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(18): Show |
21 | HG01257.hp1 HG01433.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.93+3974dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | ||||||
| chr15:41336999 | CT | C | 94 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(91): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.93+3974delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | ||||||
| chr15:41336999 | CTT | C | 19 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0001g0241 others(16): Show |
19 | HG00642.hp1 HG01074.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.93+3973_93+3974del others(2): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41336999 | ||||||
| chr15:41337009 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01175.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.93+3959T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337009 | |||||||
| chr15:41337257 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.93+4207G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337257 | |||||||
| chr15:41337264 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.93+4214G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337264 | |||||||
| chr15:41337304 | A | C | 113 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0168 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.93+4254A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337304 | |||||||
| chr15:41337391 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93+4341C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337391 | |||||||
| chr15:41337776 | C | T | 2 | a0002c0002t0001g0182 a0002c0002t0001g0183 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.94-4610C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337776 | |||||||
| chr15:41337931 | C | CT | 48 | a0001c0001t0001g0127 a0001c0001t0001g0140 a0001c0001t0001g0171 others(45): Show |
49 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.94-4436dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41337931 | ||||||
| chr15:41337931 | CT | C | 58 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0027 others(55): Show |
59 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.94-4436delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41337931 | ||||||
| chr15:41337941 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.94-4445T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41337941 | |||||||
| chr15:41338002 | G | A | 6 | a0002c0002t0001g0010 a0002c0002t0001g0237 a0002c0002t0001g0238 others(3): Show |
7 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-4384G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338002 | |||||||
| chr15:41338097 | T | C | 1 | a0001c0001t0001g0003 | 2 | NA19058.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.94-4289T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338097 | |||||||
| chr15:41338131 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-4255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338131 | |||||||
| chr15:41338301 | C | G | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-4085C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338301 | |||||||
| chr15:41338347 | C | G | 14 | a0002c0002t0001g0197 a0002c0002t0004g0009 a0002c0002t0004g0015 others(11): Show |
15 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.94-4039C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338347 | |||||||
| chr15:41338395 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.94-3991A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338395 | |||||||
| chr15:41338572 | T | C | 66 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0182 others(63): Show |
67 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.94-3814T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338572 | |||||||
| chr15:41338639 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-3747C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338639 | |||||||
| chr15:41338785 | G | A | 47 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0168 others(44): Show |
48 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.94-3601G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338785 | |||||||
| chr15:41338793 | T | TA | 44 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0032 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.94-3579dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41338793 | ||||||
| chr15:41338866 | G | A | 25 | a0002c0002t0001g0199 a0002c0002t0003g0200 a0002c0002t0003g0203 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.94-3520G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338866 | |||||||
| chr15:41338904 | G | A | 1 | a0002c0002t0003g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94-3482G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338904 | |||||||
| chr15:41338977 | T | A | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-3409T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41338977 | |||||||
| chr15:41339081 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94-3305C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339081 | |||||||
| chr15:41339209 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94-3177G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339209 | |||||||
| chr15:41339339 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-3047A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339339 | |||||||
| chr15:41339382 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94-3004T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339382 | |||||||
| chr15:41339404 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.94-2982G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339404 | |||||||
| chr15:41339411 | C | CT | 22 | a0001c0001t0001g0114 a0002c0002t0001g0197 a0002c0002t0004g0009 others(19): Show |
23 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.94-2959dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41339411 | ||||||
| chr15:41339411 | CT | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0035 a0001c0001t0001g0131 others(5): Show |
8 | HG00323.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.94-2959delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | 41339411 | ||||||
| chr15:41339485 | A | G | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.94-2901A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339485 | |||||||
| chr15:41339657 | G | A | 3 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0002g0201 |
3 | HG02723.hp2 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.94-2729G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339657 | |||||||
| chr15:41339843 | G | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.94-2543G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339843 | |||||||
| chr15:41339850 | C | T | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.94-2536C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339850 | |||||||
| chr15:41339851 | G | A | 47 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0168 others(44): Show |
48 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.94-2535G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339851 | |||||||
| chr15:41339969 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.94-2417C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41339969 | |||||||
| chr15:41340253 | C | T | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.94-2133C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340253 | |||||||
| chr15:41340301 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94-2085G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340301 | |||||||
| chr15:41340343 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.94-2043C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340343 | |||||||
| chr15:41340384 | G | A | 7 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0002g0039 others(4): Show |
7 | HG02040.hp1 NA18973.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-2002G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340384 | |||||||
| chr15:41340513 | GC | G | 11 | a0002c0002t0001g0206 a0002c0002t0001g0207 a0002c0002t0002g0201 others(8): Show |
11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.94-1872delC | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340513 | |||||||
| chr15:41340592 | T | C | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.94-1794T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41340592 | |||||||
| chr15:41341140 | A | G | 1 | a0002c0002t0003g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.94-1246A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341140 | |||||||
| chr15:41341193 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.94-1193G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341193 | |||||||
| chr15:41341725 | A | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.94-661A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341725 | |||||||
| chr15:41341872 | C | G | 223 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0022 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.94-514C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341872 | |||||||
| chr15:41341872 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94-514C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341872 | |||||||
| chr15:41341877 | C | A | 1 | a0001c0001t0002g0155 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.94-509C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341877 | |||||||
| chr15:41341907 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94-479A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41341907 | |||||||
| chr15:41342009 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.94-377A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342009 | |||||||
| chr15:41342138 | C | A | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.94-248C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342138 | |||||||
| chr15:41342311 | G | A | 1 | a0002c0002t0002g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94-75G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342311 | |||||||
| chr15:41342375 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94-11C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 1/10 | chr15 | 41342375 | |||||||
| chr15:41342481 | G | T | 1 | a0001c0001t0002g0043 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.162+27G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342481 | |||||||
| chr15:41342491 | A | G | 12 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(9): Show |
13 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.162+37A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342491 | |||||||
| chr15:41342576 | G | A | 56 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0038 others(53): Show |
60 | HG00558.hp1 HG00609.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.162+122G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342576 | |||||||
| chr15:41342581 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.162+127T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342581 | |||||||
| chr15:41342794 | G | A | 1 | a0002c0004t0004g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+340G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342794 | |||||||
| chr15:41342917 | G | C | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+463G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41342917 | |||||||
| chr15:41343026 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.162+572C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343026 | |||||||
| chr15:41343266 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0002g0164 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.162+812C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343266 | |||||||
| chr15:41343427 | T | A | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+973T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343427 | |||||||
| chr15:41343699 | C | A | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.162+1245C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343699 | |||||||
| chr15:41343729 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.162+1275G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343729 | |||||||
| chr15:41343836 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162+1382A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343836 | |||||||
| chr15:41343944 | G | A | 1 | a0002c0002t0001g0249 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.162+1490G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41343944 | |||||||
| chr15:41344190 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.162+1736G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344190 | |||||||
| chr15:41344213 | CA | C | 22 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0064 others(19): Show |
23 | HG01081.hp2 HG01106.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.162+1778delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41344213 | ||||||
| chr15:41344213 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0007g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.162+1768_162+1778d others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41344213 | ||||||
| chr15:41344238 | A | G | 1 | a0002c0002t0006g0230 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.162+1784A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344238 | |||||||
| chr15:41344463 | C | T | 47 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0165 others(44): Show |
48 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.162+2009C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344463 | |||||||
| chr15:41344587 | G | A | 38 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+2133G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344587 | |||||||
| chr15:41344669 | A | G | 58 | a0002c0002t0001g0182 a0002c0002t0001g0183 a0002c0002t0001g0184 others(55): Show |
59 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.162+2215A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344669 | |||||||
| chr15:41344880 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.162+2426G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41344880 | |||||||
| chr15:41345165 | A | G | 1 | a0001c0001t0002g0008 | 2 | HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.162+2711A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345165 | |||||||
| chr15:41345188 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.162+2734C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345188 | |||||||
| chr15:41345327 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.162+2873G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345327 | |||||||
| chr15:41345349 | T | C | 38 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0001g0207 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+2895T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345349 | |||||||
| chr15:41345408 | A | C | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.162+2954A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345408 | |||||||
| chr15:41345468 | C | CT | 7 | a0001c0001t0002g0034 a0003c0003t0005g0176 a0003c0003t0005g0177 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.162+3026dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41345468 | ||||||
| chr15:41345468 | CT | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+3026delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41345468 | ||||||
| chr15:41345944 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.163-3154A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41345944 | |||||||
| chr15:41346535 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.163-2563A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346535 | |||||||
| chr15:41346557 | G | A | 6 | a0002c0002t0001g0206 a0002c0002t0002g0201 a0002c0002t0002g0202 others(3): Show |
6 | HG00642.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-2541G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346557 | |||||||
| chr15:41346708 | T | A | 1 | a0002c0002t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.163-2390T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346708 | |||||||
| chr15:41346792 | A | C | 1 | a0001c0001t0002g0042 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163-2306A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346792 | |||||||
| chr15:41346808 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0106 |
2 | HG02735.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.163-2290C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346808 | |||||||
| chr15:41346816 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.163-2282G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346816 | |||||||
| chr15:41346826 | CAAAAATA others(2): Show |
C | 25 | a0002c0002t0001g0165 a0002c0002t0001g0168 a0002c0002t0001g0239 others(22): Show |
25 | HG00544.hp2 HG01106.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.163-2271_163-2263d others(11): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | |||||||
| chr15:41346826 | CAAAAATA others(6): Show |
C | 12 | a0002c0002t0001g0011 a0002c0002t0001g0241 a0002c0002t0001g0242 others(9): Show |
12 | HG00099.hp1 HG00609.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.163-2271_163-2259d others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | |||||||
| chr15:41346826 | CAAAAATA others(10): Show |
C | 12 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0237 others(9): Show |
13 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-2271_163-2255d others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346826 | |||||||
| chr15:41346828 | AAAAT | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
110 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.163-2220_163-2217d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | ||||||
| chr15:41346828 | AAAATAAA others(1): Show |
A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0020 others(61): Show |
66 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.163-2224_163-2217d others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | ||||||
| chr15:41346828 | AAAATAAA others(5): Show |
A | 47 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0129 others(44): Show |
48 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.163-2228_163-2217d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | ||||||
| chr15:41346828 | AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0061 a0001c0001t0002g0085 |
2 | HG02129.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.163-2232_163-2217d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41346828 | ||||||
| chr15:41346853 | A | C | 1 | a0003c0003t0005g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.163-2245A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41346853 | |||||||
| chr15:41347045 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.163-2053A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347045 | |||||||
| chr15:41347439 | C | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0263 others(1): Show |
4 | HG00609.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-1659C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347439 | |||||||
| chr15:41347515 | A | G | 1 | a0001c0001t0004g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.163-1583A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347515 | |||||||
| chr15:41347572 | T | C | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.163-1526T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347572 | |||||||
| chr15:41347608 | GATCGAGA others(2): Show |
G | 4 | a0002c0002t0002g0211 a0002c0002t0002g0212 a0002c0002t0002g0213 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-1486_163-1478d others(11): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347608 | ||||||
| chr15:41347677 | G | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-1421G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347677 | |||||||
| chr15:41347745 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0045 others(2): Show |
7 | NA18960.hp1 NA18970.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-1353T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347745 | |||||||
| chr15:41347807 | C | G | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.163-1291C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347807 | |||||||
| chr15:41347813 | C | CA | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0129 others(3): Show |
6 | HG00544.hp1 HG00642.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-1269dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347813 | ||||||
| chr15:41347813 | CA | C | 76 | a0001c0001t0001g0171 a0001c0001t0002g0029 a0002c0002t0001g0010 others(73): Show |
78 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.163-1269delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr15 | 41347813 | ||||||
| chr15:41347973 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.163-1125T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41347973 | |||||||
| chr15:41348044 | G | T | 1 | a0002c0002t0004g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.163-1054G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348044 | |||||||
| chr15:41348374 | G | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.163-724G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348374 | |||||||
| chr15:41348377 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.163-721T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348377 | |||||||
| chr15:41348454 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0035 others(1): Show |
6 | HG00558.hp2 HG02080.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-644G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348454 | |||||||
| chr15:41348838 | A | G | 1 | a0002c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.163-260A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348838 | |||||||
| chr15:41348892 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.163-206C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 2/10 | chr15 | 41348892 | |||||||
| chr15:41349261 | C | G | 1 | a0001c0001t0002g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.306+20C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349261 | |||||||
| chr15:41349345 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.306+104A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349345 | |||||||
| chr15:41349766 | C | CT | 37 | a0001c0001t0001g0137 a0001c0001t0002g0162 a0002c0002t0001g0183 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.306+542dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr15 | 41349766 | ||||||
| chr15:41349838 | C | G | 25 | a0002c0002t0001g0199 a0002c0002t0003g0200 a0002c0002t0003g0203 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.306+597C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41349838 | |||||||
| chr15:41350227 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.307-761G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350227 | |||||||
| chr15:41350356 | A | G | 1 | a0002c0002t0003g0227 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.307-632A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350356 | |||||||
| chr15:41350418 | G | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.307-570G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350418 | |||||||
| chr15:41350539 | T | C | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.307-449T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350539 | |||||||
| chr15:41350728 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.307-260T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350728 | |||||||
| chr15:41350832 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.307-156A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350832 | |||||||
| chr15:41350897 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.307-91C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 3/10 | chr15 | 41350897 | |||||||
| chr15:41351161 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+32C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351161 | |||||||
| chr15:41351162 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+33T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351162 | |||||||
| chr15:41351165 | A | T | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.448+36A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351165 | |||||||
| chr15:41351376 | C | T | 1 | a0002c0004t0004g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.448+247C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351376 | |||||||
| chr15:41351467 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.448+338G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351467 | |||||||
| chr15:41351925 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0002g0161 |
2 | NA19058.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.448+796A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41351925 | |||||||
| chr15:41351947 | CT | C | 27 | a0001c0001t0001g0028 a0001c0001t0001g0163 a0002c0002t0001g0199 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.448+832delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41351947 | ||||||
| chr15:41352100 | G | C | 1 | a0002c0002t0003g0227 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.448+971G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352100 | |||||||
| chr15:41352163 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.448+1034C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352163 | |||||||
| chr15:41352250 | G | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.448+1121G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352250 | |||||||
| chr15:41352503 | T | G | 1 | a0002c0002t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.448+1374T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352503 | |||||||
| chr15:41352575 | A | G | 1 | a0001c0001t0002g0008 | 2 | HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.448+1446A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352575 | |||||||
| chr15:41352581 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.448+1452A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352581 | |||||||
| chr15:41352615 | G | T | 3 | a0002c0002t0003g0200 a0002c0002t0003g0225 a0002c0002t0003g0226 |
3 | HG00639.hp1 HG01358.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.448+1486G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352615 | |||||||
| chr15:41352671 | C | CT | 3 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0104 |
3 | HG03225.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.448+1543dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41352671 | ||||||
| chr15:41352895 | T | C | 2 | a0002c0004t0004g0195 a0002c0004t0004g0198 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.448+1766T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41352895 | |||||||
| chr15:41353173 | CAG | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG02572.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+2047_448+2048d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41353173 | ||||||
| chr15:41353207 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.448+2078G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353207 | |||||||
| chr15:41353222 | C | A | 1 | a0002c0002t0001g0250 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.448+2093C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353222 | |||||||
| chr15:41353228 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0002g0162 |
2 | NA18998.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.448+2099G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353228 | |||||||
| chr15:41353554 | G | A | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.448+2425G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353554 | |||||||
| chr15:41353679 | A | G | 1 | a0002c0002t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.449-2360A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353679 | |||||||
| chr15:41353996 | A | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.449-2043A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41353996 | |||||||
| chr15:41354132 | T | C | 1 | a0002c0004t0004g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449-1907T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354132 | |||||||
| chr15:41354175 | A | G | 3 | a0002c0002t0002g0202 a0002c0002t0002g0209 a0002c0002t0002g0210 |
3 | HG00642.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.449-1864A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354175 | |||||||
| chr15:41354200 | C | T | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.449-1839C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354200 | |||||||
| chr15:41354223 | C | T | 13 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1816C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354223 | |||||||
| chr15:41354361 | C | T | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.449-1678C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354361 | |||||||
| chr15:41354434 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.449-1605G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354434 | |||||||
| chr15:41354670 | G | GATATAT | 13 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.449-1354_449-1349d others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | ||||||
| chr15:41354670 | G | GATATATA others(5): Show |
1 | a0002c0004t0004g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.449-1360_449-1349d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | ||||||
| chr15:41354670 | GAT | G | 149 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.449-1350_449-1349d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | ||||||
| chr15:41354670 | GATAT | G | 54 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0038 others(51): Show |
58 | HG00558.hp1 HG00609.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.449-1352_449-1349d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41354670 | ||||||
| chr15:41354976 | C | T | 3 | a0002c0002t0001g0199 a0002c0002t0006g0014 a0002c0002t0006g0230 |
3 | HG02300.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.449-1063C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354976 | |||||||
| chr15:41354998 | C | T | 6 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-1041C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41354998 | |||||||
| chr15:41355005 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.449-1034G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355005 | |||||||
| chr15:41355062 | C | G | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.449-977C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355062 | |||||||
| chr15:41355122 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.449-917T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355122 | |||||||
| chr15:41355472 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0154 |
2 | HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.449-567C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355472 | |||||||
| chr15:41355577 | T | C | 62 | a0002c0002t0001g0184 a0002c0002t0001g0197 a0002c0002t0001g0199 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.449-462T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355577 | |||||||
| chr15:41355655 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.449-384C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355655 | |||||||
| chr15:41355656 | GT | G | 111 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(108): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.449-372delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr15 | 41355656 | ||||||
| chr15:41355662 | T | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.449-377T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355662 | |||||||
| chr15:41355762 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.449-277C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355762 | |||||||
| chr15:41355925 | G | A | 2 | a0002c0002t0001g0206 a0002c0002t0002g0201 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.449-114G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 4/10 | chr15 | 41355925 | |||||||
| chr15:41356244 | C | A | 1 | a0002c0002t0008g0217 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.550+104C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356244 | |||||||
| chr15:41356354 | C | CT | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
206 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.550+232dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41356354 | ||||||
| chr15:41356354 | C | CTT | 59 | a0001c0001t0001g0049 a0001c0001t0001g0061 a0001c0001t0001g0062 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.550+231_550+232dup others(2): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41356354 | ||||||
| chr15:41356512 | G | A | 1 | a0002c0002t0003g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.550+372G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356512 | |||||||
| chr15:41356539 | C | G | 55 | a0002c0002t0001g0184 a0002c0002t0001g0199 a0002c0002t0001g0206 others(52): Show |
56 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.550+399C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356539 | |||||||
| chr15:41356583 | G | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.550+443G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356583 | |||||||
| chr15:41356608 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+468C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356608 | |||||||
| chr15:41356769 | C | G | 112 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.550+629C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356769 | |||||||
| chr15:41356925 | A | G | 1 | a0002c0002t0003g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.550+785A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41356925 | |||||||
| chr15:41357069 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.550+929T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357069 | |||||||
| chr15:41357097 | G | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.550+957G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357097 | |||||||
| chr15:41357307 | G | T | 2 | a0002c0002t0001g0261 a0002c0002t0001g0262 |
2 | HG02165.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.551-842G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357307 | |||||||
| chr15:41357449 | C | A | 1 | a0002c0002t0003g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.551-700C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357449 | |||||||
| chr15:41357588 | C | T | 2 | a0003c0003t0005g0178 a0003c0003t0005g0181 |
2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.551-561C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357588 | |||||||
| chr15:41357595 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.551-554C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357595 | |||||||
| chr15:41357622 | T | G | 2 | a0001c0001t0001g0018 a0002c0004t0004g0198 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.551-527T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357622 | |||||||
| chr15:41357682 | G | A | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.551-467G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357682 | |||||||
| chr15:41357724 | GT | G | 112 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.551-423delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | 41357724 | ||||||
| chr15:41357757 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.551-392C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357757 | |||||||
| chr15:41357855 | T | C | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.551-294T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 5/10 | chr15 | 41357855 | |||||||
| chr15:41358308 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.660+50A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358308 | |||||||
| chr15:41358313 | G | C | 1 | a0002c0002t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.660+55G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358313 | |||||||
| chr15:41358487 | C | T | 13 | a0002c0002t0001g0165 a0002c0002t0001g0239 a0002c0002t0001g0240 others(10): Show |
13 | HG01928.hp1 HG01975.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.660+229C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358487 | |||||||
| chr15:41358488 | G | A | 4 | a0002c0002t0001g0253 a0002c0002t0001g0254 a0002c0002t0001g0255 others(1): Show |
4 | NA18955.hp1 NA18968.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+230G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358488 | |||||||
| chr15:41358498 | A | G | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+240A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358498 | |||||||
| chr15:41358535 | A | C | 1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+277A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358535 | |||||||
| chr15:41358628 | A | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+370A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358628 | |||||||
| chr15:41358673 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.660+415G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358673 | |||||||
| chr15:41358689 | G | A | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+431G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358689 | |||||||
| chr15:41358690 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.660+432C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358690 | |||||||
| chr15:41358729 | G | A | 13 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.660+471G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41358729 | |||||||
| chr15:41359039 | T | C | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+781T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359039 | |||||||
| chr15:41359280 | C | T | 2 | a0002c0004t0004g0195 a0002c0004t0004g0198 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.660+1022C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359280 | |||||||
| chr15:41359371 | T | C | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.660+1113T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359371 | |||||||
| chr15:41359413 | G | A | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1155G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359413 | |||||||
| chr15:41359523 | A | G | 113 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(110): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.660+1265A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359523 | |||||||
| chr15:41359593 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1335C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359593 | |||||||
| chr15:41359617 | A | AT | 49 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(46): Show |
50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.660+1367dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41359617 | ||||||
| chr15:41359636 | C | CT | 6 | a0002c0002t0001g0197 a0002c0002t0002g0152 a0002c0002t0002g0211 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+1390dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41359636 | ||||||
| chr15:41359643 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.660+1385T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359643 | |||||||
| chr15:41359695 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.660+1437A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359695 | |||||||
| chr15:41359778 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.660+1520G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359778 | |||||||
| chr15:41359821 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.660+1563C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359821 | |||||||
| chr15:41359880 | A | G | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+1622A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359880 | |||||||
| chr15:41359892 | G | A | 49 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(46): Show |
50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.660+1634G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41359892 | |||||||
| chr15:41360021 | C | T | 4 | a0002c0002t0002g0211 a0002c0002t0002g0212 a0002c0002t0002g0213 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.660+1763C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360021 | |||||||
| chr15:41360050 | C | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.660+1792C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360050 | |||||||
| chr15:41360246 | C | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0119 |
2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.660+1988C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360246 | |||||||
| chr15:41360269 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+2011C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360269 | |||||||
| chr15:41360307 | T | TTTTG | 43 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.660+2073_660+2076d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360307 | ||||||
| chr15:41360358 | C | T | 1 | a0002c0002t0004g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+2100C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360358 | |||||||
| chr15:41360415 | C | G | 1 | a0002c0002t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.660+2157C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360415 | |||||||
| chr15:41360646 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.660+2388G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360646 | |||||||
| chr15:41360732 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.660+2474C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360732 | |||||||
| chr15:41360768 | A | G | 1 | a0002c0002t0004g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+2510A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360768 | |||||||
| chr15:41360793 | C | CT | 19 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0056 others(16): Show |
19 | HG00639.hp2 HG01169.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.660+2555dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360793 | ||||||
| chr15:41360793 | CT | C | 17 | a0001c0001t0001g0125 a0001c0001t0001g0134 a0002c0002t0001g0243 others(14): Show |
18 | HG00639.hp1 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.660+2555delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41360793 | ||||||
| chr15:41360796 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.660+2538T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360796 | |||||||
| chr15:41360826 | A | G | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+2568A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360826 | |||||||
| chr15:41360908 | G | A | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.660+2650G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41360908 | |||||||
| chr15:41361120 | G | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.660+2862G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361120 | |||||||
| chr15:41361334 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.660+3076G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361334 | |||||||
| chr15:41361358 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.660+3100A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361358 | |||||||
| chr15:41361404 | T | A | 59 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0197 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.660+3146T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361404 | |||||||
| chr15:41361633 | G | A | 11 | a0002c0002t0001g0206 a0002c0002t0002g0152 a0002c0002t0002g0201 others(8): Show |
11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+3375G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361633 | |||||||
| chr15:41361640 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.660+3382G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361640 | |||||||
| chr15:41361644 | GAACGACT others(5): Show |
G | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.660+3390_660+3401d others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41361644 | ||||||
| chr15:41361703 | A | AATAGTTT others(9): Show |
1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+3446_660+3461d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41361703 | ||||||
| chr15:41361814 | A | G | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.660+3556A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361814 | |||||||
| chr15:41361819 | T | C | 1 | a0002c0002t0003g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.660+3561T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361819 | |||||||
| chr15:41361868 | C | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-3534C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361868 | |||||||
| chr15:41361980 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.661-3422T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41361980 | |||||||
| chr15:41362336 | A | T | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-3066A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362336 | |||||||
| chr15:41362419 | C | CT | 17 | a0001c0001t0001g0060 a0001c0001t0001g0102 a0001c0001t0001g0103 others(14): Show |
18 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.661-2967dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362419 | ||||||
| chr15:41362419 | CT | C | 86 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.661-2967delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362419 | ||||||
| chr15:41362444 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.661-2958G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362444 | |||||||
| chr15:41362509 | C | T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0125 a0001c0001t0002g0091 |
3 | HG01169.hp2 HG01175.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.661-2893C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362509 | |||||||
| chr15:41362534 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.661-2868C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362534 | |||||||
| chr15:41362557 | T | C | 1 | a0002c0002t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.661-2845T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362557 | |||||||
| chr15:41362566 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0116 |
2 | HG02738.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.661-2836G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362566 | |||||||
| chr15:41362585 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2817C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362585 | |||||||
| chr15:41362603 | T | G | 107 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(104): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.661-2799T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362603 | |||||||
| chr15:41362603 | T | TG | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2798dupG | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362603 | ||||||
| chr15:41362666 | G | A | 36 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(33): Show |
36 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.661-2736G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362666 | |||||||
| chr15:41362682 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.661-2720G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362682 | |||||||
| chr15:41362720 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0073 |
2 | HG02015.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.661-2682G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362720 | |||||||
| chr15:41362806 | C | A | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2596C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362806 | |||||||
| chr15:41362835 | A | T | 5 | a0002c0002t0003g0205 a0002c0002t0003g0216 a0002c0002t0003g0218 others(2): Show |
5 | HG02602.hp1 HG03834.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-2567A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362835 | |||||||
| chr15:41362874 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.661-2528G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362874 | |||||||
| chr15:41362889 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.661-2513C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362889 | |||||||
| chr15:41362904 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG03017.hp1 HG03239.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.661-2498C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362904 | |||||||
| chr15:41362958 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.661-2444G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41362958 | |||||||
| chr15:41362976 | AATGTATA others(9): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.661-2424_661-2409d others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41362976 | ||||||
| chr15:41363099 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.661-2303C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363099 | |||||||
| chr15:41363108 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.661-2294G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363108 | |||||||
| chr15:41363237 | T | G | 223 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0022 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.661-2165T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363237 | |||||||
| chr15:41363242 | C | T | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-2160C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363242 | |||||||
| chr15:41363276 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.661-2126T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363276 | |||||||
| chr15:41363325 | G | C | 96 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.661-2077G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363325 | |||||||
| chr15:41363327 | C | G | 8 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0132 others(5): Show |
8 | HG02129.hp2 HG02976.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.661-2075C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363327 | |||||||
| chr15:41363335 | C | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.661-2067C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363335 | |||||||
| chr15:41363337 | C | A | 4 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 others(1): Show |
4 | HG01496.hp2 HG02451.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-2065C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363337 | |||||||
| chr15:41363339 | C | A | 39 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0104 others(36): Show |
39 | HG00099.hp1 HG00642.hp1 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.661-2063C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363339 | |||||||
| chr15:41363341 | A | C | 4 | a0001c0001t0001g0158 a0002c0002t0001g0197 a0002c0002t0001g0249 others(1): Show |
4 | HG01106.hp2 HG02486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.661-2061A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363341 | |||||||
| chr15:41363375 | C | CAT | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-2016_661-2015d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr15 | 41363375 | ||||||
| chr15:41363386 | A | T | 18 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 others(15): Show |
19 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.661-2016A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363386 | |||||||
| chr15:41363590 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.661-1812C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363590 | |||||||
| chr15:41363610 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.661-1792C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363610 | |||||||
| chr15:41363926 | G | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.661-1476G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41363926 | |||||||
| chr15:41364120 | A | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661-1282A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364120 | |||||||
| chr15:41364209 | G | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-1193G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364209 | |||||||
| chr15:41364306 | G | T | 1 | a0002c0002t0003g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.661-1096G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364306 | |||||||
| chr15:41364460 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.661-942C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364460 | |||||||
| chr15:41364861 | C | G | 1 | a0001c0001t0004g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661-541C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364861 | |||||||
| chr15:41364946 | T | A | 122 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0104 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.661-456T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41364946 | |||||||
| chr15:41365065 | A | C | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-337A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365065 | |||||||
| chr15:41365155 | T | C | 62 | a0002c0002t0001g0184 a0002c0002t0001g0197 a0002c0002t0001g0199 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.661-247T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365155 | |||||||
| chr15:41365299 | G | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG02145.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.661-103G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 6/10 | chr15 | 41365299 | |||||||
| chr15:41365654 | T | A | 2 | a0002c0002t0003g0225 a0002c0002t0003g0226 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.848+65T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41365654 | |||||||
| chr15:41366100 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+511T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366100 | |||||||
| chr15:41366118 | C | A | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+529C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366118 | |||||||
| chr15:41366148 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.848+559G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366148 | |||||||
| chr15:41366252 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.848+663C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366252 | |||||||
| chr15:41366291 | C | CT | 61 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(58): Show |
63 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.848+716dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41366291 | ||||||
| chr15:41366291 | CT | C | 8 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0206 others(5): Show |
8 | HG00642.hp1 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+716delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41366291 | ||||||
| chr15:41366482 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(59): Show |
68 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.848+893A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366482 | |||||||
| chr15:41366571 | C | T | 1 | a0002c0002t0001g0244 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.848+982C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366571 | |||||||
| chr15:41366585 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.848+996C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41366585 | |||||||
| chr15:41367079 | G | A | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.848+1490G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367079 | |||||||
| chr15:41367131 | C | T | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1542C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367131 | |||||||
| chr15:41367166 | C | T | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1577C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367166 | |||||||
| chr15:41367303 | T | C | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.848+1714T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367303 | |||||||
| chr15:41367443 | G | A | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.848+1854G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367443 | |||||||
| chr15:41367524 | A | T | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.848+1935A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367524 | |||||||
| chr15:41367652 | CTTGGGTA others(11): Show |
C | 1 | a0001c0001t0002g0012 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.848+2064_848+2081d others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367652 | |||||||
| chr15:41367942 | T | G | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.848+2353T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367942 | |||||||
| chr15:41367997 | A | T | 1 | a0002c0002t0003g0205 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.848+2408A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41367997 | |||||||
| chr15:41368118 | G | A | 1 | a0002c0002t0001g0279 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.848+2529G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368118 | |||||||
| chr15:41368142 | A | G | 1 | a0002c0005t0004g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.848+2553A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368142 | |||||||
| chr15:41368168 | A | G | 49 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(46): Show |
50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.848+2579A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368168 | |||||||
| chr15:41368596 | A | G | 13 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(10): Show |
14 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.849-2931A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368596 | |||||||
| chr15:41368635 | T | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-2892T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41368635 | |||||||
| chr15:41368728 | C | CT | 45 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0132 others(42): Show |
46 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.849-2775dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | ||||||
| chr15:41368728 | C | CTTT | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-2777_849-2775d others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | ||||||
| chr15:41368728 | CT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
130 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.849-2775delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | ||||||
| chr15:41368728 | CTT | C | 10 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0027 others(7): Show |
10 | HG00639.hp2 HG00741.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-2776_849-2775d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | ||||||
| chr15:41368728 | CTTT | C | 33 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.849-2777_849-2775d others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41368728 | ||||||
| chr15:41369149 | G | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.849-2378G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369149 | |||||||
| chr15:41369263 | C | T | 1 | a0002c0002t0001g0183 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2264C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369263 | |||||||
| chr15:41369403 | C | T | 24 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 others(21): Show |
25 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.849-2124C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369403 | |||||||
| chr15:41369621 | C | G | 49 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(46): Show |
50 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.849-1906C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369621 | |||||||
| chr15:41369626 | CA | C | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-1899delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41369626 | ||||||
| chr15:41369665 | A | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02015.hp1 HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.849-1862A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369665 | |||||||
| chr15:41369761 | T | C | 11 | a0002c0002t0001g0206 a0002c0002t0002g0152 a0002c0002t0002g0201 others(8): Show |
11 | HG00642.hp1 HG02055.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-1766T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369761 | |||||||
| chr15:41369800 | G | T | 1 | a0001c0001t0002g0142 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.849-1727G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41369800 | |||||||
| chr15:41370056 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.849-1471G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370056 | |||||||
| chr15:41370119 | C | A | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.849-1408C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370119 | |||||||
| chr15:41370157 | G | A | 1 | a0002c0002t0002g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.849-1370G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370157 | |||||||
| chr15:41370337 | G | A | 1 | a0002c0002t0003g0219 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.849-1190G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370337 | |||||||
| chr15:41370405 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.849-1122C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370405 | |||||||
| chr15:41370575 | A | C | 1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-952A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370575 | |||||||
| chr15:41370576 | C | A | 1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-951C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370576 | |||||||
| chr15:41370711 | T | C | 1 | a0002c0004t0004g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.849-816T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370711 | |||||||
| chr15:41370733 | G | A | 1 | a0002c0002t0003g0226 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.849-794G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370733 | |||||||
| chr15:41370749 | C | CA | 11 | a0001c0001t0001g0049 a0001c0001t0001g0060 a0001c0001t0001g0092 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.849-755dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | ||||||
| chr15:41370749 | CA | C | 30 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0093 others(27): Show |
32 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.849-755delA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | ||||||
| chr15:41370749 | CAAAAAAA others(3): Show |
C | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.849-764_849-755del others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41370749 | ||||||
| chr15:41370799 | A | G | 1 | a0002c0002t0003g0222 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.849-728A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370799 | |||||||
| chr15:41370858 | G | A | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.849-669G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41370858 | |||||||
| chr15:41371084 | C | G | 6 | a0002c0002t0001g0010 a0002c0002t0001g0237 a0002c0002t0001g0238 others(3): Show |
7 | HG02280.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-443C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371084 | |||||||
| chr15:41371086 | C | G | 1 | a0001c0001t0001g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.849-441C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371086 | |||||||
| chr15:41371163 | T | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02015.hp1 HG02132.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.849-364T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371163 | |||||||
| chr15:41371181 | C | T | 1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-346C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371181 | |||||||
| chr15:41371182 | T | A | 1 | a0002c0002t0001g0269 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.849-345T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371182 | |||||||
| chr15:41371187 | T | TGGA | 7 | a0002c0002t0001g0280 a0003c0003t0005g0176 a0003c0003t0005g0177 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-318_849-316dup others(3): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr15 | 41371187 | ||||||
| chr15:41371195 | G | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0054 a0001c0001t0001g0089 others(15): Show |
18 | HG00140.hp1 HG01169.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.849-332G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371195 | |||||||
| chr15:41371300 | G | A | 4 | a0002c0002t0001g0253 a0002c0002t0001g0254 a0002c0002t0001g0255 others(1): Show |
4 | NA18955.hp1 NA18968.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-227G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 7/10 | chr15 | 41371300 | |||||||
| chr15:41371698 | A | C | 111 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(108): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1006+14A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371698 | |||||||
| chr15:41371702 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1006+18C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371702 | |||||||
| chr15:41371714 | G | T | 1 | a0002c0004t0004g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1006+30G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371714 | |||||||
| chr15:41371753 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1006+69G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371753 | |||||||
| chr15:41371770 | G | T | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006+86G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371770 | |||||||
| chr15:41371864 | A | G | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006+180A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41371864 | |||||||
| chr15:41372048 | G | A | 1 | a0002c0004t0004g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1006+364G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372048 | |||||||
| chr15:41372187 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1006+503T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372187 | |||||||
| chr15:41372191 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1006+507C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372191 | |||||||
| chr15:41372225 | CTCCAGGA others(30): Show |
C | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0071 |
3 | NA18970.hp1 NA19056.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1006+542_1006+578d others(39): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372225 | |||||||
| chr15:41372270 | G | A | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1006+586G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372270 | |||||||
| chr15:41372327 | C | T | 2 | a0002c0002t0001g0244 a0002c0002t0001g0268 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1006+643C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372327 | |||||||
| chr15:41372494 | TTAAACAT others(1): Show |
T | 5 | a0001c0001t0002g0029 a0001c0001t0002g0072 a0001c0001t0002g0079 others(2): Show |
5 | NA18943.hp1 NA18959.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+812_1006+819d others(10): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41372494 | ||||||
| chr15:41372874 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1006+1190G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372874 | |||||||
| chr15:41372963 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1006+1279C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41372963 | |||||||
| chr15:41373224 | T | C | 1 | a0002c0002t0001g0259 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1006+1540T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373224 | |||||||
| chr15:41373250 | C | T | 7 | a0001c0001t0001g0119 a0003c0003t0005g0176 a0003c0003t0005g0177 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+1566C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373250 | |||||||
| chr15:41373251 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1006+1567G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373251 | |||||||
| chr15:41373334 | G | A | 1 | a0001c0001t0002g0012 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1650G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373334 | |||||||
| chr15:41373378 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1006+1694G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373378 | |||||||
| chr15:41373391 | T | G | 1 | a0001c0001t0002g0012 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1707T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373391 | |||||||
| chr15:41373443 | A | C | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006+1759A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373443 | |||||||
| chr15:41373448 | C | CT | 93 | a0001c0001t0001g0121 a0001c0001t0001g0138 a0001c0001t0001g0167 others(90): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1006+1783dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41373448 | ||||||
| chr15:41373448 | C | CTT | 13 | a0002c0002t0001g0206 a0002c0002t0001g0260 a0002c0002t0002g0152 others(10): Show |
13 | HG00642.hp1 HG00741.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.1006+1782_1006+178 others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41373448 | ||||||
| chr15:41373448 | C | T | 1 | a0001c0001t0002g0012 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1006+1764C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373448 | |||||||
| chr15:41373891 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1007-1821G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41373891 | |||||||
| chr15:41374005 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1007-1707C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374005 | |||||||
| chr15:41374178 | G | T | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1007-1534G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374178 | |||||||
| chr15:41374209 | A | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0060 others(3): Show |
6 | HG01168.hp2 HG01346.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-1503A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374209 | |||||||
| chr15:41374313 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1007-1399A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374313 | |||||||
| chr15:41374518 | A | G | 37 | a0002c0002t0001g0199 a0002c0002t0001g0206 a0002c0002t0002g0152 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1007-1194A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374518 | |||||||
| chr15:41374725 | C | T | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1007-987C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41374725 | |||||||
| chr15:41375008 | AT | A | 7 | a0002c0002t0003g0203 a0003c0003t0005g0176 a0003c0003t0005g0177 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-692delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375008 | ||||||
| chr15:41375128 | G | C | 2 | a0002c0004t0004g0195 a0002c0004t0004g0198 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1007-584G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375128 | |||||||
| chr15:41375135 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1007-577C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375135 | |||||||
| chr15:41375153 | A | G | 1 | a0002c0002t0003g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1007-559A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375153 | |||||||
| chr15:41375164 | C | T | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-548C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375164 | |||||||
| chr15:41375174 | AT | A | 50 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0027 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1007-517delT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375174 | ||||||
| chr15:41375174 | ATT | A | 63 | a0002c0002t0001g0010 a0002c0002t0001g0011 a0002c0002t0001g0165 others(60): Show |
65 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.1007-518_1007-517d others(4): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr15 | 41375174 | ||||||
| chr15:41375239 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1007-473G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375239 | |||||||
| chr15:41375260 | C | T | 1 | a0002c0002t0003g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1007-452C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375260 | |||||||
| chr15:41375271 | G | A | 1 | a0002c0002t0003g0224 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1007-441G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375271 | |||||||
| chr15:41375367 | G | A | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1007-345G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375367 | |||||||
| chr15:41375428 | G | A | 20 | a0002c0002t0001g0199 a0002c0002t0003g0200 a0002c0002t0003g0203 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.1007-284G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375428 | |||||||
| chr15:41375456 | G | A | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1007-256G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375456 | |||||||
| chr15:41375460 | G | A | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-252G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375460 | |||||||
| chr15:41375472 | C | A | 4 | a0002c0002t0002g0211 a0002c0002t0002g0212 a0002c0002t0002g0213 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-240C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375472 | |||||||
| chr15:41375556 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1007-156C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 8/10 | chr15 | 41375556 | |||||||
| chr15:41375885 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0002g0153 |
2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1123+57G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41375885 | |||||||
| chr15:41376012 | G | T | 6 | a0002c0002t0001g0206 a0002c0002t0002g0201 a0002c0002t0002g0202 others(3): Show |
6 | HG00642.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1123+184G>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376012 | |||||||
| chr15:41376116 | C | T | 1 | a0002c0002t0002g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1123+288C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376116 | |||||||
| chr15:41376117 | G | A | 1 | a0002c0004t0004g0198 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1123+289G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376117 | |||||||
| chr15:41376120 | C | T | 1 | a0002c0002t0001g0275 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1123+292C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376120 | |||||||
| chr15:41376171 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1123+343A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376171 | |||||||
| chr15:41376224 | C | T | 1 | a0002c0004t0004g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1123+396C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376224 | |||||||
| chr15:41376394 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1123+566G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376394 | |||||||
| chr15:41376413 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18959.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1123+585C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376413 | |||||||
| chr15:41376601 | G | A | 15 | a0002c0002t0004g0009 a0002c0002t0004g0015 a0002c0002t0004g0185 others(12): Show |
16 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1124-595G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376601 | |||||||
| chr15:41376699 | A | T | 1 | a0002c0002t0004g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1124-497A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376699 | |||||||
| chr15:41376707 | A | G | 1 | a0001c0001t0007g0173 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1124-489A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376707 | |||||||
| chr15:41376726 | T | TA | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1124-460dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr15 | 41376726 | ||||||
| chr15:41376727 | A | T | 1 | a0002c0002t0003g0218 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1124-469A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376727 | |||||||
| chr15:41376903 | C | T | 1 | a0002c0002t0004g0015 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1124-293C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376903 | |||||||
| chr15:41376918 | A | C | 4 | a0002c0002t0002g0211 a0002c0002t0002g0212 a0002c0002t0002g0213 others(1): Show |
4 | HG02055.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1124-278A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41376918 | |||||||
| chr15:41377078 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1124-118C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 9/10 | chr15 | 41377078 | |||||||
| chr15:41377423 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1232+119T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377423 | |||||||
| chr15:41377425 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1232+121T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377425 | |||||||
| chr15:41377482 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1232+178G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377482 | |||||||
| chr15:41377488 | A | G | 1 | a0002c0002t0003g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1232+184A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377488 | |||||||
| chr15:41377496 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1232+192G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377496 | |||||||
| chr15:41377555 | T | C | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+251T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377555 | |||||||
| chr15:41377558 | G | C | 1 | a0002c0002t0001g0255 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+254G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377558 | |||||||
| chr15:41377559 | C | A | 1 | a0002c0002t0001g0255 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+255C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377559 | |||||||
| chr15:41377559 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377559 | |||||||
| chr15:41377560 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1232+256A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377560 | |||||||
| chr15:41377560 | A | G | 8 | a0001c0001t0001g0116 a0002c0002t0001g0255 a0003c0003t0005g0176 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1232+256A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377560 | |||||||
| chr15:41377616 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1232+312G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377616 | |||||||
| chr15:41377624 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0002g0065 |
2 | NA18984.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1232+320A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377624 | |||||||
| chr15:41377668 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1232+364T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377668 | |||||||
| chr15:41377690 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1232+386C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377690 | |||||||
| chr15:41377698 | C | CA | 20 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0027 others(17): Show |
21 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1232+407dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41377698 | ||||||
| chr15:41377727 | A | T | 2 | a0002c0002t0001g0249 a0002c0002t0001g0258 |
2 | HG01106.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1232+423A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377727 | |||||||
| chr15:41377731 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0002c0002t0001g0249 others(1): Show |
4 | HG01106.hp2 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232+427A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377731 | |||||||
| chr15:41377732 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1232+428C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377732 | |||||||
| chr15:41377792 | C | CAGG | 16 | a0001c0001t0001g0158 a0001c0001t0001g0163 a0001c0001t0001g0167 others(13): Show |
20 | HG00609.hp2 HG01109.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1232+490_1232+491i others(5): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41377792 | ||||||
| chr15:41377792 | C | G | 1 | a0001c0001t0002g0161 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1232+488C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377792 | |||||||
| chr15:41377808 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1232+504T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377808 | |||||||
| chr15:41377816 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0002g0068 a0001c0001t0002g0069 others(2): Show |
5 | HG02559.hp2 HG03239.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1232+512G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377816 | |||||||
| chr15:41377829 | A | G | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+525A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377829 | |||||||
| chr15:41377930 | C | T | 6 | a0003c0003t0005g0176 a0003c0003t0005g0177 a0003c0003t0005g0178 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1232+626C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377930 | |||||||
| chr15:41377988 | T | C | 25 | a0002c0002t0001g0199 a0002c0002t0001g0275 a0002c0002t0003g0200 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1232+684T>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377988 | |||||||
| chr15:41377990 | A | C | 1 | a0002c0002t0003g0227 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1232+686A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41377990 | |||||||
| chr15:41378093 | C | T | 1 | a0002c0002t0002g0209 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1232+789C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378093 | |||||||
| chr15:41378145 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1232+841C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378145 | |||||||
| chr15:41378190 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1232+886G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378190 | |||||||
| chr15:41378210 | C | G | 25 | a0002c0002t0001g0199 a0002c0002t0003g0200 a0002c0002t0003g0203 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1232+906C>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378210 | |||||||
| chr15:41378265 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1232+961C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378265 | |||||||
| chr15:41378323 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1232+1019G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378323 | |||||||
| chr15:41378335 | C | T | 1 | a0002c0002t0001g0255 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1232+1031C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378335 | |||||||
| chr15:41378541 | T | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1232+1237T>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378541 | |||||||
| chr15:41378579 | T | A | 3 | a0002c0002t0001g0184 a0002c0002t0001g0235 a0002c0002t0001g0236 |
3 | HG01496.hp2 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1232+1275T>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378579 | |||||||
| chr15:41378581 | G | C | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1277G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378581 | |||||||
| chr15:41378582 | A | T | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1278A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378582 | |||||||
| chr15:41378583 | A | T | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1279A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378583 | |||||||
| chr15:41378584 | G | C | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1232+1280G>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378584 | |||||||
| chr15:41378899 | C | CA | 14 | a0001c0001t0004g0105 a0002c0002t0004g0009 a0002c0002t0004g0015 others(11): Show |
15 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1233-1182dupA | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378899 | ||||||
| chr15:41378905 | A | G | 2 | a0002c0002t0001g0240 a0002c0002t0001g0270 |
2 | NA18964.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1233-1188A>G | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378905 | |||||||
| chr15:41378944 | G | GGTT | 5 | a0001c0001t0004g0105 a0002c0002t0004g0015 a0002c0002t0004g0187 others(2): Show |
5 | HG03041.hp1 HG04199.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | |||||||
| chr15:41378944 | G | GGTTT | 6 | a0002c0002t0004g0009 a0002c0002t0004g0185 a0002c0002t0004g0186 others(3): Show |
7 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | |||||||
| chr15:41378944 | G | GGTTTT | 4 | a0002c0002t0004g0188 a0002c0002t0004g0192 a0002c0004t0004g0195 others(1): Show |
4 | HG01517.hp1 HG02615.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233-1149_1233-114 others(9): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41378944 | |||||||
| chr15:41378944 | G | GT | 31 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(28): Show |
33 | HG00639.hp2 HG01175.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1233-1122dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTT | 51 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0027 others(48): Show |
55 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1233-1123_1233-112 others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTT | 42 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0033 others(39): Show |
42 | HG00140.hp1 HG01109.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1233-1124_1233-112 others(7): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTT | 10 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0102 others(7): Show |
10 | HG01496.hp2 HG02027.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1233-1125_1233-112 others(8): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTGTT others(7): Show |
1 | a0003c0003t0005g0179 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1233-1145_1233-114 others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTGTT others(8): Show |
4 | a0003c0003t0005g0176 a0003c0003t0005g0178 a0003c0003t0005g0180 others(1): Show |
4 | HG01109.hp1 HG01243.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233-1145_1233-114 others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTGTT others(9): Show |
1 | a0003c0003t0005g0177 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1233-1145_1233-114 others(20): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(2): Show |
7 | a0002c0002t0001g0010 a0002c0002t0001g0242 a0002c0002t0001g0255 others(4): Show |
8 | HG01975.hp2 NA18522.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233-1130_1233-112 others(13): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(3): Show |
14 | a0002c0002t0001g0165 a0002c0002t0001g0237 a0002c0002t0001g0245 others(11): Show |
14 | HG02004.hp2 HG02273.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-1131_1233-112 others(14): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(4): Show |
14 | a0002c0002t0001g0011 a0002c0002t0001g0238 a0002c0002t0001g0239 others(11): Show |
14 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233-1132_1233-112 others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(5): Show |
22 | a0001c0001t0001g0171 a0002c0002t0001g0241 a0002c0002t0001g0243 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1233-1133_1233-112 others(16): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(6): Show |
11 | a0002c0002t0002g0208 a0002c0002t0002g0210 a0002c0002t0003g0200 others(8): Show |
11 | HG00323.hp2 HG00741.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233-1134_1233-112 others(17): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(7): Show |
7 | a0002c0002t0001g0199 a0002c0002t0001g0261 a0002c0002t0002g0212 others(4): Show |
7 | HG00642.hp2 HG02258.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233-1135_1233-112 others(18): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(8): Show |
1 | a0002c0002t0002g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233-1136_1233-112 others(19): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | G | GTTTTTTT others(11): Show |
1 | a0002c0002t0001g0262 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1233-1139_1233-112 others(22): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41378944 | GTTTTTTT others(4): Show |
G | 2 | a0002c0002t0001g0206 a0002c0002t0002g0201 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1233-1132_1233-112 others(15): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41378944 | ||||||
| chr15:41379020 | C | T | 1 | a0002c0002t0001g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1233-1073C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379020 | |||||||
| chr15:41379247 | C | A | 1 | a0001c0001t0002g0039 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1233-846C>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379247 | |||||||
| chr15:41379295 | A | AT | 18 | a0001c0001t0004g0105 a0002c0002t0001g0206 a0002c0002t0001g0255 others(15): Show |
19 | HG01081.hp2 HG01106.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1233-785dupT | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41379295 | ||||||
| chr15:41379535 | TTTTA | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0027 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233-555_1233-552d others(6): Show |
NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr15 | 41379535 | ||||||
| chr15:41379542 | A | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0252 a0002c0002t0001g0263 others(1): Show |
4 | HG00609.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233-551A>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379542 | |||||||
| chr15:41379576 | A | C | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1233-517A>C | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379576 | |||||||
| chr15:41379838 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1233-255C>T | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379838 | |||||||
| chr15:41379839 | G | A | 48 | a0001c0001t0001g0171 a0002c0002t0001g0010 a0002c0002t0001g0011 others(45): Show |
49 | HG00099.hp1 HG00609.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.1233-254G>A | NUSAP1 | ENSG00000137804.14 | transcript | ENST00000559596.6 | protein_coding | 10/10 | chr15 | 41379839 |