Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84081 |
| ensemblid | ENSG00000126653.18 |
| hgncid | 25305 |
| symbol | NSRP1 |
| name | nuclear speckle splicing regulatory protein 1 |
| refseq_nuc | NM_032141.4 |
| refseq_prot | NP_115517.1 |
| ensembl_nuc | ENST00000247026.10 |
| ensembl_prot | ENSP00000247026.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 30116816 |
| end | 30186475 |
| strand | + |
| ver | v1.2 |
| region | chr17:30116816-30186475 |
| region5000 | chr17:30111816-30191475 |
| regionname0 | NSRP1_chr17_30116816_30186475 |
| regionname5000 | NSRP1_chr17_30111816_30191475 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 558 | 258 | 89 | 51 | 67 | 12 | 37 | 56 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0002 | 0/0 | 558 | 7 | 0 | 4 | 3 | 0 | 0 | 2 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0003 | 0/0 | 558 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0004 | 0/0 | 558 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0005 | 0/0 | 558 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0006 | 0/0 | 558 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0007 | 0/0 | 558 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0008 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0009 | 0/0 | 558 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0010 | 0/0 | 558 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| a0011 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | MAIPG others(553): Show |
chr17 | 30111816 | 30191475 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1674 | 129 | 43 | 30 | 34 | 4 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0001c0002 | 1/1 | 1674 | 125 | 43 | 21 | 33 | 8 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0001c0008 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0001c0009 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0001c0011 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0001c0014 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0002c0003 | 0/0 | 1674 | 7 | 0 | 4 | 3 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0003c0005 | 0/0 | 1674 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0003c0012 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0004c0006 | 0/0 | 1674 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0005c0004 | 0/0 | 1674 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0006c0007 | 0/0 | 1674 | 2 | 0 | 0 | 2 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0007c0015 | 0/0 | 1674 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0008c0010 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0009c0017 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0010c0016 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 | ||
| a0011c0013 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | ATGGC others(1669): Show |
chr17 | 30111816 | 30191475 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2506 | 26 | 24 | 2 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0001t0002 | 0/0 | 2506 | 94 | 13 | 25 | 34 | 4 | 18 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0001t0004 | 0/0 | 2506 | 4 | 3 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0001t0005 | 0/0 | 2506 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0001t0006 | 0/0 | 2506 | 2 | 0 | 2 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0002t0001 | 1/1 | 2506 | 104 | 28 | 16 | 33 | 8 | 17 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0002t0003 | 0/0 | 2506 | 18 | 13 | 5 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | AGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0002t0007 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0002t0009 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0008t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0009t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0011t0002 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0001c0014t0008 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0002c0003t0001 | 0/0 | 2506 | 7 | 0 | 4 | 3 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0003c0005t0001 | 0/0 | 2506 | 3 | 3 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0003c0012t0002 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0004c0006t0001 | 0/0 | 2506 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0005c0004t0001 | 0/0 | 2506 | 3 | 0 | 2 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0006c0007t0002 | 0/0 | 2506 | 2 | 0 | 0 | 2 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0007c0015t0001 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0008c0010t0001 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0009c0017t0003 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | AGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0010c0016t0001 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| a0011c0013t0002 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | GGCCA others(2501): Show |
chr17 | 30111816 | 30191475 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0008t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0009t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0011t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0001c0014t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0003c0005t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0003c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0003c0005t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0003c0012t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0004c0006t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0004c0006t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0004c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0005c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0005c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0005c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0006c0007t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0006c0007t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0007c0015t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0008c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0009c0017t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0010c0016t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| a0011c0013t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0006 | t0001 | g0120 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0102 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0087 | EUR | GBR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00280 | hp1 | a0005 | c0004 | t0001 | g0062 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0057 | EUR | FIN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0028 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01070 | hp2 | a0005 | c0004 | t0001 | g0048 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01071 | hp1 | a0005 | c0004 | t0001 | g0049 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0029 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0036 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01168 | hp1 | a0007 | c0015 | t0001 | g0064 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0111 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0080 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0275 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01496 | hp2 | a0004 | c0006 | t0001 | g0058 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0270 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0271 | EUR | IBS | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0070 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0051 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0052 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02055 | hp2 | a0001 | c0009 | t0001 | g0156 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02129 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02280 | hp1 | a0001 | c0002 | t0003 | g0030 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0038 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02818 | hp2 | a0001 | c0002 | t0003 | g0034 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0265 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02976 | hp1 | a0001 | c0008 | t0001 | g0163 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03017 | hp2 | a0001 | c0002 | t0009 | g0069 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0081 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03486 | hp1 | a0008 | c0010 | t0001 | g0150 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | ESN | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03579 | hp1 | a0009 | c0017 | t0003 | g0079 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03669 | hp2 | a0010 | c0016 | t0001 | g0060 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03704 | hp1 | a0001 | c0011 | t0002 | g0191 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0089 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | STU | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18906 | hp2 | a0003 | c0005 | t0001 | g0266 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18948 | hp2 | a0006 | c0007 | t0002 | g0260 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18988 | hp2 | a0006 | c0007 | t0002 | g0173 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18993 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19011 | hp2 | a0011 | c0013 | t0002 | g0205 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0082 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19054 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19067 | hp1 | a0003 | c0012 | t0002 | g0256 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0107 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | YRI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ASW | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20129 | hp2 | a0003 | c0005 | t0001 | g0264 | AFR | ASW | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0059 | EUR | TSI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0238 | EUR | TSI | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | GIH | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | GIH | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01123 | hp1 | a0004 | c0006 | t0001 | g0043 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0274 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02559 | hp1 | a0001 | c0014 | t0008 | g0121 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG06807 | hp1 | a0001 | c0002 | t0007 | g0112 | AFR | USA | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | USA | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | LWK | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0040 | REF | REF | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0075 | REF | REF | NSRP1_chr17_30111816_30191475 | NSRP1 | chr17 | 30111816 | 30191475 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30178156 | A | C | 1 | a0004 | 3 | HG00099.hp1 HG01123.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.257A>C | p.Lys86Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/7 | 285/2506 | 257/1677 | 86/558 | chr17 | 30178156 | |||
| chr17:30178165 | A | G | 1 | a0009 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.266A>G | p.Asn89Ser | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/7 | 294/2506 | 266/1677 | 89/558 | chr17 | 30178165 | |||
| chr17:30184866 | G | A | 1 | a0002 | 7 | HG01346.hp2 HG01978.hp2 HG01993.hp2 others(4): Show |
missense_variant | MODERATE | c.869G>A | p.Arg290Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 897/2506 | 869/1677 | 290/558 | chr17 | 30184866 | |||
| chr17:30184978 | C | G | 1 | a0010 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.981C>G | p.Asp327Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1009/2506 | 981/1677 | 327/558 | chr17 | 30184978 | |||
| chr17:30185021 | G | A | 1 | a0008 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.1024G>A | p.Asp342Asn | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1052/2506 | 1024/1677 | 342/558 | chr17 | 30185021 | |||
| chr17:30185305 | T | G | 1 | a0006 | 2 | NA18948.hp2 NA18988.hp2 |
missense_variant | MODERATE | c.1308T>G | p.Asp436Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1336/2506 | 1308/1677 | 436/558 | chr17 | 30185305 | |||
| chr17:30185315 | C | G | 1 | a0003 | 3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.1318C>G | p.Arg440Gly | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1346/2506 | 1318/1677 | 440/558 | chr17 | 30185315 | |||
| chr17:30185316 | G | A | 1 | a0003 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.1319G>A | p.Arg440Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1347/2506 | 1319/1677 | 440/558 | chr17 | 30185316 | |||
| chr17:30185387 | G | A | 1 | a0005 | 3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
missense_variant | MODERATE | c.1390G>A | p.Asp464Asn | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1418/2506 | 1390/1677 | 464/558 | chr17 | 30185387 | |||
| chr17:30185499 | G | C | 1 | a0007 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1502G>C | p.Arg501Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1530/2506 | 1502/1677 | 501/558 | chr17 | 30185499 | |||
| chr17:30185631 | C | T | 1 | a0011 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1634C>T | p.Ala545Val | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1662/2506 | 1634/1677 | 545/558 | chr17 | 30185631 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30184840 | G | A | 1 | a0001c0008 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.843G>A | p.Lys281Lys | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 871/2506 | 843/1677 | 281/558 | chr17 | 30184840 | |||
| chr17:30184909 | G | A | 1 | a0001c0009 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.912G>A | p.Thr304Thr | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 940/2506 | 912/1677 | 304/558 | chr17 | 30184909 | |||
| chr17:30184960 | G | A | 8 | a0001c0001 a0001c0008 a0001c0009 others(5): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
synonymous_variant | LOW | c.963G>A | p.Gln321Gln | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 991/2506 | 963/1677 | 321/558 | chr17 | 30184960 | |||
| chr17:30185098 | G | A | 1 | a0001c0014 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1101G>A | p.Ala367Ala | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1129/2506 | 1101/1677 | 367/558 | chr17 | 30185098 | |||
| chr17:30185233 | G | A | 1 | a0001c0011 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1236G>A | p.Glu412Glu | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 1264/2506 | 1236/1677 | 412/558 | chr17 | 30185233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30116816 | G | A | 2 | a0001c0002t0003 a0009c0017t0003 |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-28G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/7 | 28 | chr17 | 30116816 | ||||||
| chr17:30185736 | C | T | 1 | a0001c0002t0009 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 62 | chr17 | 30185736 | ||||||
| chr17:30185745 | A | G | 1 | a0001c0002t0007 | 2 | HG06807.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 71 | chr17 | 30185745 | ||||||
| chr17:30185839 | A | G | 1 | a0001c0001t0004 | 4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 165 | chr17 | 30185839 | ||||||
| chr17:30185988 | G | A | 1 | a0001c0001t0005 | 3 | HG02922.hp2 HG03195.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*314G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 314 | chr17 | 30185988 | ||||||
| chr17:30186047 | A | T | 1 | a0001c0014t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 373 | chr17 | 30186047 | ||||||
| chr17:30186158 | G | A | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(4): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*484G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 484 | chr17 | 30186158 | ||||||
| chr17:30186430 | C | T | 1 | a0001c0001t0006 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*756C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 7/7 | 756 | chr17 | 30186430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:30117165 | A | C | 112 | a0001c0001t0002g0002 a0001c0001t0002g0170 a0001c0001t0002g0171 others(109): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.20+302A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117165 | |||||||
| chr17:30117208 | G | C | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(1): Show |
4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+345G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117208 | |||||||
| chr17:30117236 | T | A | 95 | a0001c0001t0002g0002 a0001c0001t0002g0170 a0001c0001t0002g0171 others(92): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.20+373T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117236 | |||||||
| chr17:30117756 | CAT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(18): Show |
22 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.21-323_21-322delAT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117756 | |||||||
| chr17:30117756 | CATG | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.21-323_21-321delAT others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117756 | |||||||
| chr17:30117757 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-323A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117757 | |||||||
| chr17:30117758 | TG | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-321delG | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117758 | |||||||
| chr17:30117759 | G | GT | 6 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0002t0001g0143 others(3): Show |
6 | HG02738.hp1 HG02738.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-303dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 30117759 | ||||||
| chr17:30117759 | GT | G | 19 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0002g0172 others(16): Show |
19 | HG00597.hp1 HG00741.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.21-303delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 30117759 | ||||||
| chr17:30117760 | T | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.21-320T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117760 | |||||||
| chr17:30117944 | A | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.21-136A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117944 | |||||||
| chr17:30117966 | A | G | 1 | a0001c0002t0001g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.21-114A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 1/6 | chr17 | 30117966 | |||||||
| chr17:30118199 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+26G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118199 | |||||||
| chr17:30118414 | T | TG | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+241_114+242ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118414 | |||||||
| chr17:30118556 | C | T | 2 | a0001c0001t0001g0167 a0001c0002t0001g0141 |
2 | HG02074.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.114+383C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118556 | |||||||
| chr17:30118713 | A | G | 3 | a0001c0001t0002g0261 a0006c0007t0002g0173 a0006c0007t0002g0260 |
3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+540A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118713 | |||||||
| chr17:30118749 | C | CT | 8 | a0001c0001t0002g0176 a0001c0001t0002g0258 a0001c0001t0002g0259 others(5): Show |
8 | HG02451.hp2 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+593dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30118749 | ||||||
| chr17:30118749 | CT | C | 13 | a0001c0001t0001g0151 a0001c0001t0002g0177 a0001c0001t0002g0178 others(10): Show |
13 | HG01070.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.114+593delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30118749 | ||||||
| chr17:30118750 | T | TC | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+577_114+578ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118750 | |||||||
| chr17:30118751 | T | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+578T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118751 | |||||||
| chr17:30118879 | G | C | 4 | a0001c0002t0001g0024 a0001c0002t0001g0025 a0001c0002t0001g0026 others(1): Show |
4 | HG02109.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+706G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30118879 | |||||||
| chr17:30119119 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+946C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119119 | |||||||
| chr17:30119208 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+1035A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119208 | |||||||
| chr17:30119401 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.114+1228C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119401 | |||||||
| chr17:30119508 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.114+1335G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119508 | |||||||
| chr17:30119525 | T | C | 1 | a0001c0001t0002g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.114+1352T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119525 | |||||||
| chr17:30119583 | A | T | 1 | a0001c0002t0001g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.114+1410A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119583 | |||||||
| chr17:30119619 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1446C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119619 | |||||||
| chr17:30119785 | G | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+1612G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30119785 | |||||||
| chr17:30120072 | C | T | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+1899C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120072 | |||||||
| chr17:30120076 | C | T | 4 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0128 others(1): Show |
4 | HG02622.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+1903C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120076 | |||||||
| chr17:30120082 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1909C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120082 | |||||||
| chr17:30120085 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+1912A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120085 | |||||||
| chr17:30120123 | T | C | 2 | a0001c0002t0001g0137 a0001c0002t0001g0138 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114+1950T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120123 | |||||||
| chr17:30120235 | AT | A | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+2068delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30120235 | ||||||
| chr17:30120320 | A | C | 3 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 |
3 | NA18951.hp1 NA18972.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.114+2147A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120320 | |||||||
| chr17:30120347 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+2174A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120347 | |||||||
| chr17:30120381 | C | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2208C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120381 | |||||||
| chr17:30120388 | A | G | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+2215A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120388 | |||||||
| chr17:30120552 | T | TA | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2380dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30120552 | ||||||
| chr17:30120664 | G | A | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+2491G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120664 | |||||||
| chr17:30120872 | C | T | 1 | a0004c0006t0001g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.114+2699C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30120872 | |||||||
| chr17:30121035 | C | T | 4 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0118 others(1): Show |
4 | HG01952.hp2 HG02273.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+2862C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121035 | |||||||
| chr17:30121094 | T | C | 1 | a0001c0002t0001g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.114+2921T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121094 | |||||||
| chr17:30121394 | AG | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+3222delG | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121394 | |||||||
| chr17:30121453 | C | CT | 14 | a0001c0001t0001g0153 a0001c0001t0001g0164 a0001c0001t0002g0254 others(11): Show |
14 | HG01069.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+3296dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121453 | ||||||
| chr17:30121453 | CT | C | 5 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(2): Show |
5 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+3296delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121453 | ||||||
| chr17:30121570 | G | GT | 60 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.114+3412dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | ||||||
| chr17:30121570 | G | GTT | 6 | a0001c0001t0002g0263 a0001c0001t0002g0280 a0001c0002t0001g0113 others(3): Show |
6 | HG00609.hp1 HG02145.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+3411_114+3412d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | ||||||
| chr17:30121570 | GT | G | 20 | a0001c0002t0001g0023 a0001c0002t0001g0267 a0001c0002t0001g0268 others(17): Show |
20 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+3412delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121570 | ||||||
| chr17:30121591 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+3418G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121591 | |||||||
| chr17:30121676 | TCTC | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(24): Show |
28 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.114+3506_114+3508d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30121676 | ||||||
| chr17:30121819 | C | T | 6 | a0001c0001t0002g0245 a0001c0001t0002g0246 a0001c0001t0002g0247 others(3): Show |
6 | HG00597.hp2 NA18954.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+3646C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121819 | |||||||
| chr17:30121860 | G | T | 1 | a0001c0002t0001g0085 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.114+3687G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30121860 | |||||||
| chr17:30122017 | G | T | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.114+3844G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122017 | |||||||
| chr17:30122253 | T | G | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.114+4080T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122253 | |||||||
| chr17:30122348 | GTTTCA | G | 6 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4177_114+4181d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122348 | ||||||
| chr17:30122348 | GTTTCATA others(4): Show |
G | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+4177_114+4187d others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122348 | ||||||
| chr17:30122349 | T | TGTG | 7 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+4176_114+4177i others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | |||||||
| chr17:30122349 | T | TGTGTG | 3 | a0001c0001t0001g0133 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG01891.hp2 HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.114+4176_114+4177i others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | |||||||
| chr17:30122349 | T | TGTGTGTG others(14): Show |
1 | a0001c0001t0005g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.114+4176_114+4177i others(23): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | |||||||
| chr17:30122349 | T | TGTGTGTG others(18): Show |
1 | a0001c0001t0005g0155 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.114+4176_114+4177i others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122349 | |||||||
| chr17:30122350 | T | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0158 a0001c0001t0001g0162 |
3 | HG02717.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.114+4177T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122350 | |||||||
| chr17:30122351 | T | A | 3 | a0001c0001t0001g0133 a0001c0001t0005g0154 a0001c0001t0005g0155 |
3 | HG02723.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.114+4178T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | |||||||
| chr17:30122351 | T | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(7): Show |
11 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+4178T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | |||||||
| chr17:30122351 | TC | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4179delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122351 | |||||||
| chr17:30122352 | C | CAT | 5 | a0001c0002t0001g0014 a0001c0002t0001g0024 a0001c0002t0001g0109 others(2): Show |
5 | HG00597.hp1 HG01081.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4212_114+4213d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATAT | 10 | a0001c0001t0002g0182 a0001c0001t0002g0194 a0001c0001t0002g0206 others(7): Show |
10 | HG01361.hp2 HG01496.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+4208_114+4213d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(1): Show |
5 | a0001c0001t0002g0183 a0001c0001t0002g0200 a0001c0001t0002g0240 others(2): Show |
5 | HG02602.hp1 HG04115.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+4206_114+4213d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(3): Show |
9 | a0001c0001t0002g0198 a0001c0001t0002g0208 a0001c0001t0002g0215 others(6): Show |
9 | HG00639.hp2 HG00733.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.114+4204_114+4213d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(5): Show |
3 | a0001c0001t0002g0211 a0001c0001t0002g0213 a0001c0001t0002g0253 |
3 | HG00280.hp2 HG03239.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.114+4202_114+4213d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(7): Show |
3 | a0001c0001t0002g0199 a0001c0001t0002g0222 a0001c0001t0002g0249 |
3 | HG02273.hp1 HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.114+4200_114+4213d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(9): Show |
1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114+4198_114+4213d others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(11): Show |
1 | a0001c0001t0002g0192 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.114+4196_114+4213d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(13): Show |
1 | a0001c0001t0002g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.114+4194_114+4213d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | CATATATA others(41): Show |
1 | a0001c0001t0002g0209 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(50): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | C | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(11): Show |
15 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4179C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122352 | |||||||
| chr17:30122352 | CAT | C | 5 | a0001c0002t0001g0022 a0001c0002t0001g0078 a0001c0002t0001g0123 others(2): Show |
5 | HG02004.hp1 HG03834.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4212_114+4213d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | CATAT | C | 5 | a0001c0001t0002g0196 a0001c0002t0001g0074 a0001c0002t0001g0099 others(2): Show |
5 | HG00639.hp1 HG01993.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+4210_114+4213d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122352 | CATATAT | C | 3 | a0001c0002t0001g0042 a0001c0002t0001g0057 a0001c0002t0001g0068 |
3 | HG00323.hp2 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4213d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122352 | ||||||
| chr17:30122353 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
10 | HG01934.hp2 HG02717.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4180A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122353 | |||||||
| chr17:30122355 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0135 a0001c0001t0001g0151 others(11): Show |
15 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4182A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122355 | |||||||
| chr17:30122357 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+4184A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122357 | |||||||
| chr17:30122359 | A | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0165 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4186A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122359 | |||||||
| chr17:30122361 | A | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0161 a0001c0001t0001g0164 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4188A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122361 | |||||||
| chr17:30122363 | A | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0161 a0001c0001t0005g0157 others(1): Show |
4 | HG02055.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+4190A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122363 | |||||||
| chr17:30122365 | A | G | 2 | a0001c0001t0001g0153 a0001c0009t0001g0156 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4192A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122365 | |||||||
| chr17:30122367 | A | G | 2 | a0001c0001t0001g0153 a0001c0009t0001g0156 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4194A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122367 | |||||||
| chr17:30122369 | A | G | 2 | a0001c0001t0001g0153 a0001c0009t0001g0156 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+4196A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122369 | |||||||
| chr17:30122369 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0002g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114+4198_114+4217d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122369 | ||||||
| chr17:30122369 | ATATATAT others(26): Show |
A | 1 | a0001c0002t0003g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.114+4198_114+4230d others(35): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122369 | ||||||
| chr17:30122371 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+4198A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122371 | |||||||
| chr17:30122371 | ATATATAT others(25): Show |
A | 18 | a0001c0002t0003g0016 a0001c0002t0003g0027 a0001c0002t0003g0028 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.114+4200_114+4231d others(34): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122371 | ||||||
| chr17:30122373 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.114+4200A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122373 | |||||||
| chr17:30122373 | ATATATAT others(23): Show |
A | 1 | a0001c0002t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+4202_114+4231d others(32): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122373 | ||||||
| chr17:30122373 | ATATATAT others(24): Show |
A | 6 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(3): Show |
6 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4202_114+4232d others(33): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122373 | ||||||
| chr17:30122375 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0004g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.114+4204_114+4214d others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122375 | ||||||
| chr17:30122377 | ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114+4206_114+4217d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | ||||||
| chr17:30122377 | ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0207 |
2 | HG00609.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.114+4206_114+4218d others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | ||||||
| chr17:30122377 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0002g0172 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.114+4206_114+4219d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | ||||||
| chr17:30122377 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+4206_114+4223d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122377 | ||||||
| chr17:30122379 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4228d others(23): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122379 | ||||||
| chr17:30122379 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+4208_114+4229d others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122379 | ||||||
| chr17:30122380 | TATATA | T | 3 | a0001c0002t0001g0041 a0001c0002t0001g0065 a0001c0002t0001g0087 |
3 | HG00140.hp2 HG00733.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.114+4208_114+4212d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122380 | |||||||
| chr17:30122383 | ATATTT | A | 5 | a0001c0001t0002g0280 a0001c0002t0001g0020 a0001c0002t0001g0054 others(2): Show |
5 | HG01261.hp1 HG01516.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+4212_114+4216d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122383 | ||||||
| chr17:30122383 | ATATTTT | A | 6 | a0001c0001t0002g0224 a0001c0002t0001g0007 a0001c0002t0001g0018 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4212_114+4217d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122383 | ||||||
| chr17:30122385 | A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0214 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0181 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0195 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | A | T | 2 | a0001c0002t0001g0078 a0001c0002t0001g0127 |
2 | HG02622.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.114+4212A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122385 | |||||||
| chr17:30122385 | AT | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(11): Show |
15 | HG00323.hp1 HG01891.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+4250delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATT | A | 9 | a0001c0002t0001g0008 a0001c0002t0001g0015 a0001c0002t0001g0025 others(6): Show |
9 | HG02630.hp2 HG03471.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+4249_114+4250d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTT | A | 14 | a0001c0001t0001g0158 a0001c0002t0001g0003 a0001c0002t0001g0056 others(11): Show |
14 | HG00642.hp2 HG01168.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+4248_114+4250d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTTT | A | 11 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0044 others(8): Show |
11 | HG00280.hp1 HG01071.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+4247_114+4250d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTTTT | A | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0002g0175 others(8): Show |
11 | HG01070.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+4246_114+4250d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTTTTT | A | 7 | a0001c0001t0001g0161 a0001c0002t0001g0013 a0001c0002t0001g0017 others(4): Show |
7 | HG01099.hp1 HG02148.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+4245_114+4250d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTTTTTT others(1): Show |
A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG01243.hp2 HG02145.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+4243_114+4250d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122385 | ATTTTTTT others(3): Show |
A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4241_114+4250d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30122385 | ||||||
| chr17:30122386 | T | TA | 9 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0002g0279 others(6): Show |
9 | HG00140.hp1 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(3): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATA | 16 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0186 others(13): Show |
16 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA | 6 | a0001c0001t0002g0188 a0001c0001t0002g0204 a0001c0001t0002g0231 others(3): Show |
6 | HG00597.hp2 HG02683.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(2): Show |
8 | a0001c0001t0002g0002 a0001c0001t0002g0084 a0001c0001t0002g0197 others(5): Show |
8 | HG01081.hp1 HG01167.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+4213_114+4214i others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(4): Show |
3 | a0001c0001t0002g0230 a0001c0001t0002g0234 a0001c0001t0002g0245 |
3 | HG02293.hp1 HG03927.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.114+4213_114+4214i others(13): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(6): Show |
2 | a0001c0001t0002g0190 a0001c0001t0002g0258 |
2 | NA18946.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.114+4213_114+4214i others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(8): Show |
1 | a0001c0001t0002g0203 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(17): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(12): Show |
1 | a0001c0001t0002g0262 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(21): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(16): Show |
1 | a0001c0001t0002g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114+4213_114+4214i others(25): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122386 | T | TATATATA others(18): Show |
1 | a0001c0002t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114+4213_114+4214i others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122386 | |||||||
| chr17:30122387 | T | A | 48 | a0001c0001t0001g0135 a0001c0001t0001g0153 a0001c0001t0001g0159 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.114+4214T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122387 | |||||||
| chr17:30122388 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(44): Show |
49 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.114+4215T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122388 | |||||||
| chr17:30122389 | T | A | 23 | a0001c0001t0001g0135 a0001c0001t0002g0183 a0001c0001t0002g0199 others(20): Show |
23 | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.114+4216T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122389 | |||||||
| chr17:30122390 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
31 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.114+4217T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122390 | |||||||
| chr17:30122391 | T | A | 12 | a0001c0001t0002g0200 a0001c0001t0002g0209 a0001c0002t0001g0008 others(9): Show |
12 | HG00597.hp1 HG02074.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+4218T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122391 | |||||||
| chr17:30122392 | T | A | 19 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(16): Show |
19 | HG00597.hp2 HG00741.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.114+4219T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122392 | |||||||
| chr17:30122393 | T | A | 4 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0026 others(1): Show |
4 | HG00597.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+4220T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122393 | |||||||
| chr17:30122394 | T | A | 10 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(7): Show |
10 | HG00597.hp2 HG01891.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4221T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122394 | |||||||
| chr17:30122395 | T | A | 3 | a0001c0001t0001g0162 a0001c0002t0001g0013 a0001c0002t0001g0026 |
3 | HG02886.hp2 HG03195.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.114+4222T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122395 | |||||||
| chr17:30122396 | T | A | 2 | a0003c0005t0001g0265 a0003c0005t0001g0266 |
2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4223T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122396 | |||||||
| chr17:30122397 | T | A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4224T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122397 | |||||||
| chr17:30122398 | T | A | 2 | a0003c0005t0001g0265 a0003c0005t0001g0266 |
2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4225T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122398 | |||||||
| chr17:30122399 | T | A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4226T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122399 | |||||||
| chr17:30122400 | T | A | 2 | a0003c0005t0001g0265 a0003c0005t0001g0266 |
2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4227T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122400 | |||||||
| chr17:30122401 | T | A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4228T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122401 | |||||||
| chr17:30122402 | T | A | 2 | a0003c0005t0001g0265 a0003c0005t0001g0266 |
2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.114+4229T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122402 | |||||||
| chr17:30122403 | T | A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4230T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122403 | |||||||
| chr17:30122404 | T | A | 1 | a0003c0005t0001g0265 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.114+4231T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122404 | |||||||
| chr17:30122405 | T | A | 1 | a0003c0005t0001g0264 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+4232T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122405 | |||||||
| chr17:30122429 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+4256G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122429 | |||||||
| chr17:30122463 | G | A | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.114+4290G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122463 | |||||||
| chr17:30122544 | A | G | 1 | a0001c0001t0002g0244 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.114+4371A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122544 | |||||||
| chr17:30122549 | C | A | 2 | a0004c0006t0001g0043 a0004c0006t0001g0120 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.114+4376C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122549 | |||||||
| chr17:30122686 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+4513G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122686 | |||||||
| chr17:30122718 | G | A | 1 | a0001c0001t0002g0251 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.114+4545G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122718 | |||||||
| chr17:30122732 | C | T | 1 | a0001c0002t0001g0015 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.114+4559C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122732 | |||||||
| chr17:30122978 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+4805T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122978 | |||||||
| chr17:30122995 | G | A | 6 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0044 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4822G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122995 | |||||||
| chr17:30122997 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+4824T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30122997 | |||||||
| chr17:30123011 | C | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0110 |
2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+4838C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123011 | |||||||
| chr17:30123052 | TGGGACTA others(64): Show |
T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+4881_114+4951d others(73): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30123052 | ||||||
| chr17:30123131 | G | A | 1 | a0001c0002t0007g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.114+4958G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123131 | |||||||
| chr17:30123274 | C | T | 2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | NA18995.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.114+5101C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123274 | |||||||
| chr17:30123871 | T | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+5698T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123871 | |||||||
| chr17:30123877 | A | G | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+5704A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30123877 | |||||||
| chr17:30124231 | C | G | 1 | a0001c0002t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+6058C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124231 | |||||||
| chr17:30124316 | A | T | 1 | a0001c0002t0001g0140 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.114+6143A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124316 | |||||||
| chr17:30124578 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.114+6405G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124578 | |||||||
| chr17:30124651 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+6478G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124651 | |||||||
| chr17:30124847 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+6674T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124847 | |||||||
| chr17:30124848 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114+6675G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124848 | |||||||
| chr17:30124919 | C | T | 1 | a0001c0002t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.114+6746C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124919 | |||||||
| chr17:30124961 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.114+6788G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30124961 | |||||||
| chr17:30125131 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+6958G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125131 | |||||||
| chr17:30125217 | T | A | 1 | a0001c0001t0002g0258 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.114+7044T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125217 | |||||||
| chr17:30125584 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.114+7411G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125584 | |||||||
| chr17:30125608 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114+7435C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125608 | |||||||
| chr17:30125635 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+7462C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125635 | |||||||
| chr17:30125986 | A | C | 1 | a0001c0001t0002g0245 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.114+7813A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30125986 | |||||||
| chr17:30126235 | GC | G | 4 | a0001c0001t0002g0183 a0003c0005t0001g0264 a0003c0005t0001g0265 others(1): Show |
4 | HG02895.hp1 NA18906.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+8066delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30126235 | ||||||
| chr17:30126287 | A | T | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+8114A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126287 | |||||||
| chr17:30126295 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.114+8122G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126295 | |||||||
| chr17:30126335 | G | C | 1 | a0001c0002t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+8162G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126335 | |||||||
| chr17:30126401 | A | C | 1 | a0001c0002t0003g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+8228A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126401 | |||||||
| chr17:30126544 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.114+8371G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126544 | |||||||
| chr17:30126709 | T | C | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+8536T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126709 | |||||||
| chr17:30126735 | G | A | 94 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.114+8562G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126735 | |||||||
| chr17:30126770 | G | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+8597G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126770 | |||||||
| chr17:30126839 | C | G | 1 | a0001c0002t0001g0085 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.114+8666C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30126839 | |||||||
| chr17:30127114 | A | G | 1 | a0001c0001t0004g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+8941A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127114 | |||||||
| chr17:30127258 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+9085C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127258 | |||||||
| chr17:30127405 | G | C | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+9232G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127405 | |||||||
| chr17:30127483 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.114+9310C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127483 | |||||||
| chr17:30127551 | C | T | 1 | a0001c0001t0004g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+9378C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127551 | |||||||
| chr17:30127604 | G | T | 4 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0243 others(1): Show |
4 | NA18947.hp2 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+9431G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127604 | |||||||
| chr17:30127807 | A | G | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(1): Show |
4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+9634A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127807 | |||||||
| chr17:30127809 | A | G | 1 | a0001c0001t0002g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.114+9636A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127809 | |||||||
| chr17:30127835 | A | T | 1 | a0001c0002t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114+9662A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30127835 | |||||||
| chr17:30128172 | T | TTA | 4 | a0001c0001t0002g0241 a0001c0001t0002g0242 a0001c0001t0002g0243 others(1): Show |
4 | NA18947.hp2 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+10012_114+1001 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30128172 | ||||||
| chr17:30128187 | A | T | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+10014A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128187 | |||||||
| chr17:30128338 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+10165A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128338 | |||||||
| chr17:30128520 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.114+10347T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128520 | |||||||
| chr17:30128657 | GATATA | G | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+10490_114+1049 others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30128657 | ||||||
| chr17:30128903 | A | C | 1 | a0001c0002t0003g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.114+10730A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30128903 | |||||||
| chr17:30129026 | G | A | 2 | a0001c0001t0001g0153 a0001c0009t0001g0156 |
2 | HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.114+10853G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129026 | |||||||
| chr17:30129047 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114+10874C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129047 | |||||||
| chr17:30129057 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+10884A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129057 | |||||||
| chr17:30129060 | AT | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+10898delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30129060 | ||||||
| chr17:30129094 | A | G | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+10921A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129094 | |||||||
| chr17:30129134 | A | G | 1 | a0001c0002t0007g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.114+10961A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129134 | |||||||
| chr17:30129181 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114+11008C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129181 | |||||||
| chr17:30129549 | A | G | 1 | a0001c0002t0003g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.114+11376A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129549 | |||||||
| chr17:30129586 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.114+11413C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129586 | |||||||
| chr17:30129682 | C | T | 5 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(2): Show |
5 | HG02572.hp2 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+11509C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129682 | |||||||
| chr17:30129719 | A | C | 2 | a0001c0002t0001g0020 a0001c0002t0001g0110 |
2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+11546A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129719 | |||||||
| chr17:30129740 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.114+11567C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129740 | |||||||
| chr17:30129793 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+11620A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129793 | |||||||
| chr17:30129963 | A | C | 1 | a0001c0001t0004g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.114+11790A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30129963 | |||||||
| chr17:30130031 | A | G | 20 | a0001c0002t0001g0022 a0001c0002t0001g0096 a0001c0002t0001g0097 others(17): Show |
20 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.114+11858A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130031 | |||||||
| chr17:30130123 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.114+11950G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130123 | |||||||
| chr17:30130205 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.114+12032C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130205 | |||||||
| chr17:30130289 | G | C | 1 | a0001c0002t0001g0096 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+12116G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130289 | |||||||
| chr17:30130602 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.114+12429A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130602 | |||||||
| chr17:30130856 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+12683T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130856 | |||||||
| chr17:30130967 | C | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+12794C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130967 | |||||||
| chr17:30130971 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+12798A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30130971 | |||||||
| chr17:30131087 | A | G | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+12914A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131087 | |||||||
| chr17:30131259 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+13086A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131259 | |||||||
| chr17:30131324 | T | TTATTTTG others(314): Show |
2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+13166_114+1316 others(325): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30131324 | ||||||
| chr17:30131700 | G | T | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114+13527G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131700 | |||||||
| chr17:30131969 | C | T | 1 | a0001c0001t0002g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.114+13796C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131969 | |||||||
| chr17:30131977 | G | C | 1 | a0001c0001t0002g0188 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+13804G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30131977 | |||||||
| chr17:30132097 | A | C | 1 | a0001c0001t0002g0248 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.114+13924A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132097 | |||||||
| chr17:30132121 | G | A | 6 | a0001c0002t0003g0016 a0001c0002t0003g0038 a0001c0002t0003g0080 others(3): Show |
6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+13948G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132121 | |||||||
| chr17:30132123 | C | CT | 15 | a0001c0001t0002g0002 a0001c0001t0002g0228 a0001c0001t0002g0230 others(12): Show |
16 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+13951dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30132123 | ||||||
| chr17:30132163 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+13990G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132163 | |||||||
| chr17:30132223 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+14050G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132223 | |||||||
| chr17:30132245 | C | CA | 23 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(20): Show |
23 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.114+14086dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30132245 | ||||||
| chr17:30132302 | C | T | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+14129C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132302 | |||||||
| chr17:30132336 | T | G | 1 | a0001c0002t0003g0027 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.114+14163T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132336 | |||||||
| chr17:30132566 | C | G | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+14393C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132566 | |||||||
| chr17:30132589 | G | C | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+14416G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132589 | |||||||
| chr17:30132689 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+14516C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132689 | |||||||
| chr17:30132894 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+14721A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132894 | |||||||
| chr17:30132981 | T | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+14808T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132981 | |||||||
| chr17:30132991 | G | C | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+14818G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30132991 | |||||||
| chr17:30133109 | A | AT | 14 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(11): Show |
14 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+14958dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | ||||||
| chr17:30133109 | AT | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(55): Show |
59 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(56): Show |
intron_variant | MODIFIER | c.114+14958delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | ||||||
| chr17:30133109 | ATT | A | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.114+14957_114+1495 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30133109 | ||||||
| chr17:30133141 | A | G | 1 | a0001c0002t0009g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.114+14968A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133141 | |||||||
| chr17:30133283 | G | A | 1 | a0001c0002t0001g0004 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.114+15110G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133283 | |||||||
| chr17:30133339 | T | A | 1 | a0001c0001t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114+15166T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133339 | |||||||
| chr17:30133380 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.114+15207C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133380 | |||||||
| chr17:30133549 | A | G | 1 | a0001c0002t0003g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114+15376A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133549 | |||||||
| chr17:30133959 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114+15786A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30133959 | |||||||
| chr17:30134039 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+15866C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134039 | |||||||
| chr17:30134237 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114+16064A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134237 | |||||||
| chr17:30134333 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.114+16160A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134333 | |||||||
| chr17:30134669 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(133): Show |
138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.114+16496T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30134669 | |||||||
| chr17:30135001 | T | TAC | 9 | a0001c0001t0002g0002 a0001c0001t0002g0228 a0001c0001t0002g0230 others(6): Show |
10 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+16829_114+1683 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30135001 | ||||||
| chr17:30135010 | A | T | 1 | a0001c0002t0009g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.114+16837A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135010 | |||||||
| chr17:30135049 | T | C | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+16876T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135049 | |||||||
| chr17:30135113 | A | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+16940A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135113 | |||||||
| chr17:30135117 | C | A | 8 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0002t0001g0007 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+16944C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135117 | |||||||
| chr17:30135121 | C | A | 1 | a0001c0001t0002g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.114+16948C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135121 | |||||||
| chr17:30135492 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+17319C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135492 | |||||||
| chr17:30135537 | G | A | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+17364G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135537 | |||||||
| chr17:30135642 | T | G | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+17469T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135642 | |||||||
| chr17:30135721 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+17548C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135721 | |||||||
| chr17:30135749 | C | T | 12 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(9): Show |
12 | HG02145.hp1 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.114+17576C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135749 | |||||||
| chr17:30135814 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.114+17641A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135814 | |||||||
| chr17:30135986 | G | A | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+17813G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30135986 | |||||||
| chr17:30136396 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+18223G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136396 | |||||||
| chr17:30136548 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.114+18375G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136548 | |||||||
| chr17:30136568 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.114+18395A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136568 | |||||||
| chr17:30136746 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114+18573C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136746 | |||||||
| chr17:30136817 | TC | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+18645delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136817 | |||||||
| chr17:30136857 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.114+18684C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136857 | |||||||
| chr17:30136875 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+18702T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30136875 | |||||||
| chr17:30137103 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+18930G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137103 | |||||||
| chr17:30137155 | T | C | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(1): Show |
4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+18982T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137155 | |||||||
| chr17:30137165 | A | G | 3 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0002t0001g0087 |
3 | HG00140.hp2 HG00733.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.114+18992A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137165 | |||||||
| chr17:30137456 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+19283T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137456 | |||||||
| chr17:30137945 | G | C | 1 | a0001c0002t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.114+19772G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137945 | |||||||
| chr17:30137988 | A | G | 3 | a0001c0002t0003g0027 a0001c0002t0003g0034 a0001c0002t0003g0035 |
3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+19815A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30137988 | |||||||
| chr17:30138160 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+19987G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138160 | |||||||
| chr17:30138258 | T | C | 3 | a0001c0001t0002g0261 a0006c0007t0002g0173 a0006c0007t0002g0260 |
3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+20085T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138258 | |||||||
| chr17:30138270 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+20097T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138270 | |||||||
| chr17:30138281 | A | G | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+20108A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138281 | |||||||
| chr17:30138364 | G | C | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+20191G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138364 | |||||||
| chr17:30138380 | T | A | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+20207T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138380 | |||||||
| chr17:30138662 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+20489G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138662 | |||||||
| chr17:30138909 | G | GT | 52 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0158 others(49): Show |
52 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.114+20762dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138909 | G | GTT | 11 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0002g0170 others(8): Show |
11 | HG01168.hp1 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+20761_114+2076 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138909 | G | GTTT | 58 | a0001c0001t0001g0166 a0001c0001t0002g0002 a0001c0001t0002g0083 others(55): Show |
59 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.114+20760_114+2076 others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138909 | G | GTTTT | 40 | a0001c0001t0002g0172 a0001c0001t0002g0176 a0001c0001t0002g0178 others(37): Show |
40 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.114+20759_114+2076 others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138909 | G | GTTTTT | 5 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0222 others(2): Show |
5 | HG00639.hp2 HG02132.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+20758_114+2076 others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138909 | GT | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(14): Show |
18 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+20762delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138909 | ||||||
| chr17:30138920 | T | G | 1 | a0001c0002t0001g0065 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.114+20747T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138920 | |||||||
| chr17:30138922 | T | TG | 6 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(3): Show |
6 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+20749_114+2075 others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138922 | |||||||
| chr17:30138943 | A | C | 1 | a0001c0002t0001g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.114+20770A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138943 | |||||||
| chr17:30138973 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0226 |
2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.114+20800A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30138973 | |||||||
| chr17:30138996 | CAAGCTCC others(184): Show |
C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+20825_114+2101 others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30138996 | ||||||
| chr17:30139098 | TAGTAGAG others(80): Show |
T | 1 | a0001c0002t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.114+20926_114+2101 others(91): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139098 | |||||||
| chr17:30139108 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.114+20935G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139108 | |||||||
| chr17:30139163 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.114+20990C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139163 | |||||||
| chr17:30139187 | G | T | 1 | a0001c0002t0001g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.114+21014G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139187 | |||||||
| chr17:30139197 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114+21024G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139197 | |||||||
| chr17:30139239 | G | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21066G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139239 | |||||||
| chr17:30139722 | G | C | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+21549G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139722 | |||||||
| chr17:30139798 | G | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21625G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139798 | |||||||
| chr17:30139806 | T | C | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+21633T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139806 | |||||||
| chr17:30139891 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114+21718G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30139891 | |||||||
| chr17:30140425 | A | G | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+22252A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140425 | |||||||
| chr17:30140520 | C | CT | 15 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(12): Show |
15 | HG00609.hp1 HG01884.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+22373dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | ||||||
| chr17:30140520 | CT | C | 116 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(113): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+22373delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | ||||||
| chr17:30140520 | CTT | C | 10 | a0001c0001t0002g0190 a0001c0001t0002g0232 a0001c0001t0002g0241 others(7): Show |
10 | HG01069.hp1 HG01069.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+22372_114+2237 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | ||||||
| chr17:30140520 | CTTTT | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(27): Show |
31 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.114+22370_114+2237 others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30140520 | ||||||
| chr17:30140590 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+22417G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140590 | |||||||
| chr17:30140605 | T | C | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.114+22432T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140605 | |||||||
| chr17:30140621 | C | G | 4 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 others(1): Show |
4 | HG02723.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+22448C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140621 | |||||||
| chr17:30140731 | T | C | 1 | a0001c0002t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.114+22558T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140731 | |||||||
| chr17:30140752 | A | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 |
4 | HG02895.hp2 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+22579A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140752 | |||||||
| chr17:30140770 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+22597C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140770 | |||||||
| chr17:30140817 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.114+22644C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140817 | |||||||
| chr17:30140831 | G | T | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+22658G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140831 | |||||||
| chr17:30140914 | A | G | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114+22741A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30140914 | |||||||
| chr17:30141161 | CTATTT | C | 3 | a0005c0004t0001g0048 a0005c0004t0001g0049 a0005c0004t0001g0062 |
3 | HG00280.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.114+22993_114+2299 others(9): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30141161 | ||||||
| chr17:30141189 | T | C | 7 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(4): Show |
7 | HG02523.hp1 HG02683.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+23016T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141189 | |||||||
| chr17:30141291 | G | A | 2 | a0001c0002t0001g0144 a0001c0002t0001g0145 |
2 | NA18940.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.114+23118G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141291 | |||||||
| chr17:30141717 | T | A | 2 | a0003c0005t0001g0264 a0003c0005t0001g0266 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+23544T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141717 | |||||||
| chr17:30141811 | C | A | 1 | a0001c0002t0001g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114+23638C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141811 | |||||||
| chr17:30141884 | G | T | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.114+23711G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30141884 | |||||||
| chr17:30142224 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114+24051A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142224 | |||||||
| chr17:30142311 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+24138T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142311 | |||||||
| chr17:30142338 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.114+24165C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142338 | |||||||
| chr17:30142483 | G | T | 2 | a0005c0004t0001g0048 a0005c0004t0001g0049 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.114+24310G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142483 | |||||||
| chr17:30142695 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+24522G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142695 | |||||||
| chr17:30142764 | T | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.114+24591T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142764 | |||||||
| chr17:30142782 | T | G | 3 | a0001c0002t0003g0027 a0001c0002t0003g0034 a0001c0002t0003g0035 |
3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+24609T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142782 | |||||||
| chr17:30142877 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+24704A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142877 | |||||||
| chr17:30142955 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.114+24782A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30142955 | |||||||
| chr17:30143042 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.114+24869A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143042 | |||||||
| chr17:30143073 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+24900T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143073 | |||||||
| chr17:30143268 | T | C | 2 | a0001c0002t0001g0137 a0001c0002t0001g0138 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114+25095T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143268 | |||||||
| chr17:30143446 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.114+25273C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143446 | |||||||
| chr17:30143456 | T | C | 1 | a0001c0001t0002g0177 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.114+25283T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143456 | |||||||
| chr17:30143475 | A | G | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+25302A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143475 | |||||||
| chr17:30143587 | T | C | 2 | a0006c0007t0002g0173 a0006c0007t0002g0260 |
2 | NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.114+25414T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143587 | |||||||
| chr17:30143846 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114+25673A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30143846 | |||||||
| chr17:30144165 | T | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+25992T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144165 | |||||||
| chr17:30144230 | C | T | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.114+26057C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144230 | |||||||
| chr17:30144247 | T | G | 1 | a0001c0002t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+26074T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144247 | |||||||
| chr17:30144260 | A | T | 6 | a0001c0001t0001g0158 a0001c0001t0002g0084 a0001c0001t0002g0206 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+26087A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144260 | |||||||
| chr17:30144263 | A | T | 72 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0158 others(69): Show |
72 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.114+26090A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144263 | |||||||
| chr17:30144264 | T | A | 1 | a0001c0001t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114+26091T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144264 | |||||||
| chr17:30144266 | A | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.114+26093A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144266 | |||||||
| chr17:30144269 | A | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.114+26096A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144269 | |||||||
| chr17:30144513 | G | A | 1 | a0001c0002t0001g0145 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.114+26340G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144513 | |||||||
| chr17:30144596 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0204 |
2 | HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.114+26423C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144596 | |||||||
| chr17:30144628 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.114+26455T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144628 | |||||||
| chr17:30144661 | A | T | 2 | a0001c0002t0001g0020 a0001c0002t0001g0110 |
2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.114+26488A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144661 | |||||||
| chr17:30144702 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.114+26529T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144702 | |||||||
| chr17:30144722 | T | C | 1 | a0001c0002t0001g0050 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.114+26549T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144722 | |||||||
| chr17:30144795 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.114+26622C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30144795 | |||||||
| chr17:30145125 | A | C | 1 | a0001c0002t0003g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.114+26952A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145125 | |||||||
| chr17:30145193 | A | G | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.114+27020A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145193 | |||||||
| chr17:30145219 | C | G | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.114+27046C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145219 | |||||||
| chr17:30145239 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02293.hp2 HG03139.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+27066G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145239 | |||||||
| chr17:30145255 | G | A | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+27082G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145255 | |||||||
| chr17:30145295 | C | A | 3 | a0001c0002t0003g0027 a0001c0002t0003g0034 a0001c0002t0003g0035 |
3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.114+27122C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145295 | |||||||
| chr17:30145322 | CCT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.114+27154_114+2715 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30145322 | ||||||
| chr17:30145342 | T | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+27169T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145342 | |||||||
| chr17:30145532 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-27010G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145532 | |||||||
| chr17:30145569 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.115-26973G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145569 | |||||||
| chr17:30145744 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-26798C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30145744 | |||||||
| chr17:30146002 | AC | A | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-26538delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30146002 | ||||||
| chr17:30146216 | C | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(1): Show |
4 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-26326C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146216 | |||||||
| chr17:30146238 | A | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-26304A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146238 | |||||||
| chr17:30146479 | T | C | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-26063T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146479 | |||||||
| chr17:30146697 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.115-25845G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146697 | |||||||
| chr17:30146748 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.115-25794G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146748 | |||||||
| chr17:30146816 | G | A | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.115-25726G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146816 | |||||||
| chr17:30146889 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.115-25653G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30146889 | |||||||
| chr17:30147132 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(128): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.115-25397dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30147132 | ||||||
| chr17:30147368 | G | A | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.115-25174G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147368 | |||||||
| chr17:30147541 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-25001G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147541 | |||||||
| chr17:30147568 | A | G | 4 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0139 others(1): Show |
4 | HG02723.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-24974A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147568 | |||||||
| chr17:30147619 | A | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-24923A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147619 | |||||||
| chr17:30147666 | T | C | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-24876T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147666 | |||||||
| chr17:30147709 | C | T | 1 | a0001c0002t0001g0014 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.115-24833C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147709 | |||||||
| chr17:30147813 | C | CT | 7 | a0001c0001t0002g0186 a0001c0001t0006g0227 a0001c0001t0006g0229 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-24714dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30147813 | ||||||
| chr17:30147916 | A | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0228 a0001c0001t0002g0230 others(11): Show |
15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-24626A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30147916 | |||||||
| chr17:30148008 | T | C | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-24534T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148008 | |||||||
| chr17:30148013 | A | G | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-24529A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148013 | |||||||
| chr17:30148033 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.115-24509G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148033 | |||||||
| chr17:30148361 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(162): Show |
167 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.115-24181G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148361 | |||||||
| chr17:30148507 | C | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-24035C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148507 | |||||||
| chr17:30148711 | G | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-23831G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30148711 | |||||||
| chr17:30149023 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-23519T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149023 | |||||||
| chr17:30149259 | G | A | 1 | a0002c0003t0001g0051 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.115-23283G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149259 | |||||||
| chr17:30149284 | G | A | 2 | a0001c0002t0001g0023 a0001c0002t0001g0050 |
2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.115-23258G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149284 | |||||||
| chr17:30149393 | A | C | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-23149A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149393 | |||||||
| chr17:30149440 | T | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-23102T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149440 | |||||||
| chr17:30149604 | G | A | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0005 others(1): Show |
4 | NA18963.hp1 NA19006.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-22938G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149604 | |||||||
| chr17:30149637 | C | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-22905C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149637 | |||||||
| chr17:30149748 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115-22794T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149748 | |||||||
| chr17:30149765 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.115-22777G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149765 | |||||||
| chr17:30149834 | C | CA | 90 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.115-22688dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | ||||||
| chr17:30149834 | C | CAA | 22 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(19): Show |
22 | HG00323.hp1 HG00597.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.115-22689_115-2268 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | ||||||
| chr17:30149834 | C | CAAA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(26): Show |
30 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.115-22690_115-2268 others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30149834 | ||||||
| chr17:30149855 | T | A | 17 | a0001c0002t0003g0016 a0001c0002t0003g0028 a0001c0002t0003g0029 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.115-22687T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149855 | |||||||
| chr17:30149979 | C | G | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-22563C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30149979 | |||||||
| chr17:30150035 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.115-22507C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150035 | |||||||
| chr17:30150069 | A | G | 2 | a0006c0007t0002g0173 a0006c0007t0002g0260 |
2 | NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.115-22473A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150069 | |||||||
| chr17:30150237 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(161): Show |
166 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.115-22305T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150237 | |||||||
| chr17:30150249 | T | A | 3 | a0001c0002t0003g0031 a0001c0002t0003g0032 a0001c0002t0003g0033 |
3 | HG02622.hp1 HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.115-22293T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150249 | |||||||
| chr17:30150310 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-22232A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150310 | |||||||
| chr17:30150461 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-22081C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150461 | |||||||
| chr17:30150480 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-22062T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150480 | |||||||
| chr17:30150543 | C | T | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-21999C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150543 | |||||||
| chr17:30150573 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21969G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150573 | |||||||
| chr17:30150684 | G | GT | 31 | a0001c0001t0001g0148 a0001c0001t0001g0164 a0001c0001t0001g0166 others(28): Show |
31 | HG01071.hp1 HG01361.hp1 HG01978.hp2 others(28): Show |
intron_variant | MODIFIER | c.115-21832dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | ||||||
| chr17:30150684 | G | GTT | 9 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
9 | HG01243.hp2 HG01891.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21833_115-2183 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | ||||||
| chr17:30150684 | GT | G | 47 | a0001c0001t0002g0170 a0001c0001t0002g0175 a0001c0001t0002g0176 others(44): Show |
47 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.115-21832delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | ||||||
| chr17:30150684 | GTT | G | 77 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.115-21833_115-2183 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30150684 | ||||||
| chr17:30150700 | T | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-21842T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150700 | |||||||
| chr17:30150714 | A | C | 1 | a0003c0005t0001g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-21828A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150714 | |||||||
| chr17:30150764 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-21778T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150764 | |||||||
| chr17:30150768 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-21774A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150768 | |||||||
| chr17:30150801 | C | T | 2 | a0001c0002t0001g0003 a0001c0002t0001g0004 |
2 | NA18963.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.115-21741C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150801 | |||||||
| chr17:30150805 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.115-21737A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150805 | |||||||
| chr17:30150929 | C | A | 24 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0089 others(21): Show |
24 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.115-21613C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150929 | |||||||
| chr17:30150940 | G | A | 1 | a0001c0002t0003g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.115-21602G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30150940 | |||||||
| chr17:30151045 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.115-21497C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151045 | |||||||
| chr17:30151126 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-21416C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151126 | |||||||
| chr17:30151170 | A | C | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-21372A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151170 | |||||||
| chr17:30151311 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-21231C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151311 | |||||||
| chr17:30151367 | A | G | 2 | a0001c0001t0002g0190 a0001c0001t0002g0209 |
2 | HG02074.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.115-21175A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151367 | |||||||
| chr17:30151375 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.115-21167G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151375 | |||||||
| chr17:30151524 | A | G | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-21018A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151524 | |||||||
| chr17:30151645 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-20897G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151645 | |||||||
| chr17:30151686 | A | G | 3 | a0001c0001t0002g0181 a0001c0001t0002g0192 a0001c0001t0002g0200 |
3 | HG03669.hp1 NA18961.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.115-20856A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151686 | |||||||
| chr17:30151717 | A | G | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-20825A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151717 | |||||||
| chr17:30151774 | C | CT | 29 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0002g0174 others(26): Show |
29 | HG00597.hp2 HG00741.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.115-20743dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30151774 | ||||||
| chr17:30151774 | CT | C | 31 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0132 others(28): Show |
31 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.115-20743delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30151774 | ||||||
| chr17:30151919 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-20623G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30151919 | |||||||
| chr17:30152069 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115-20473G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152069 | |||||||
| chr17:30152103 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0226 |
2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.115-20439A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152103 | |||||||
| chr17:30152226 | G | A | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-20316G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152226 | |||||||
| chr17:30152247 | C | T | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-20295C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152247 | |||||||
| chr17:30152304 | G | A | 1 | a0001c0002t0001g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.115-20238G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152304 | |||||||
| chr17:30152325 | C | T | 2 | a0001c0002t0001g0093 a0001c0002t0001g0095 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.115-20217C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152325 | |||||||
| chr17:30152327 | C | T | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-20215C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152327 | |||||||
| chr17:30152423 | A | AT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(43): Show |
47 | HG01168.hp2 HG01243.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.115-20100dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152423 | ||||||
| chr17:30152423 | A | ATT | 94 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.115-20101_115-2010 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152423 | ||||||
| chr17:30152586 | G | A | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-19956G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152586 | |||||||
| chr17:30152781 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(267): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.115-19761G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152781 | |||||||
| chr17:30152836 | T | C | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-19706T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30152836 | |||||||
| chr17:30152903 | C | CT | 21 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-19616dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | ||||||
| chr17:30152903 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0063 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.115-19625_115-1961 others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | ||||||
| chr17:30152903 | CT | C | 138 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.115-19616delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | ||||||
| chr17:30152903 | CTT | C | 7 | a0001c0001t0002g0172 a0001c0001t0002g0203 a0001c0001t0002g0254 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-19617_115-1961 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30152903 | ||||||
| chr17:30153007 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115-19535A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153007 | |||||||
| chr17:30153085 | T | C | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-19457T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153085 | |||||||
| chr17:30153106 | G | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-19436G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153106 | |||||||
| chr17:30153207 | G | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-19335G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153207 | |||||||
| chr17:30153400 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-19142G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153400 | |||||||
| chr17:30153824 | A | G | 1 | a0010c0016t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.115-18718A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153824 | |||||||
| chr17:30153909 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-18633C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30153909 | |||||||
| chr17:30154140 | C | T | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-18402C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154140 | |||||||
| chr17:30154181 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.115-18361T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154181 | |||||||
| chr17:30154306 | G | T | 1 | a0001c0002t0001g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.115-18236G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154306 | |||||||
| chr17:30154513 | A | G | 1 | a0010c0016t0001g0060 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.115-18029A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154513 | |||||||
| chr17:30154572 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-17970G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154572 | |||||||
| chr17:30154667 | G | A | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-17875G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154667 | |||||||
| chr17:30154819 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-17723C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30154819 | |||||||
| chr17:30155175 | G | A | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-17367G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155175 | |||||||
| chr17:30155348 | T | C | 8 | a0001c0001t0002g0178 a0001c0001t0002g0182 a0001c0001t0002g0193 others(5): Show |
8 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-17194T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155348 | |||||||
| chr17:30155440 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-17102A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155440 | |||||||
| chr17:30155470 | A | C | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-17072A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155470 | |||||||
| chr17:30155486 | A | G | 1 | a0001c0002t0001g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.115-17056A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155486 | |||||||
| chr17:30155531 | C | A | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-17011C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155531 | |||||||
| chr17:30155700 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115-16842C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155700 | |||||||
| chr17:30155780 | T | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-16762T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30155780 | |||||||
| chr17:30156039 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.115-16503C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156039 | |||||||
| chr17:30156078 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.115-16464G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156078 | |||||||
| chr17:30156092 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115-16450G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156092 | |||||||
| chr17:30156135 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-16407C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156135 | |||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
95 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(92): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
1 | a0001c0001t0002g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156248 | G | GCTGTTTA others(807): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-16292_115-1629 others(818): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30156248 | ||||||
| chr17:30156429 | A | G | 4 | a0001c0001t0001g0158 a0001c0001t0002g0174 a0001c0001t0002g0175 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-16113A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156429 | |||||||
| chr17:30156623 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.115-15919G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156623 | |||||||
| chr17:30156629 | C | G | 1 | a0001c0001t0002g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.115-15913C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156629 | |||||||
| chr17:30156739 | G | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-15803G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156739 | |||||||
| chr17:30156961 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-15581A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30156961 | |||||||
| chr17:30157133 | T | C | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-15409T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157133 | |||||||
| chr17:30157185 | C | A | 1 | a0001c0002t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.115-15357C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157185 | |||||||
| chr17:30157216 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-15326G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157216 | |||||||
| chr17:30157920 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.115-14622A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30157920 | |||||||
| chr17:30158215 | A | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-14327A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158215 | |||||||
| chr17:30158308 | A | AT | 33 | a0001c0001t0001g0134 a0001c0001t0002g0170 a0001c0001t0002g0174 others(30): Show |
33 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-14219dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30158308 | ||||||
| chr17:30158308 | A | ATT | 89 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(86): Show |
90 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.115-14220_115-1421 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30158308 | ||||||
| chr17:30158394 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-14148C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158394 | |||||||
| chr17:30158651 | CAG | C | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-13890_115-1388 others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158651 | |||||||
| chr17:30158744 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.115-13798A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30158744 | |||||||
| chr17:30159053 | G | A | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-13489G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159053 | |||||||
| chr17:30159351 | G | GT | 5 | a0001c0002t0001g0003 a0001c0002t0001g0103 a0003c0005t0001g0264 others(2): Show |
5 | HG02895.hp1 NA18906.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-13183dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30159351 | ||||||
| chr17:30159358 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.115-13184T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159358 | |||||||
| chr17:30159360 | G | T | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-13182G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159360 | |||||||
| chr17:30159368 | G | T | 1 | a0001c0001t0002g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.115-13174G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159368 | |||||||
| chr17:30159804 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0228 a0001c0001t0002g0230 others(11): Show |
15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-12738A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159804 | |||||||
| chr17:30159957 | C | T | 19 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(16): Show |
19 | HG00597.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.115-12585C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30159957 | |||||||
| chr17:30160075 | T | G | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-12467T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160075 | |||||||
| chr17:30160253 | T | G | 1 | a0001c0001t0004g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-12289T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160253 | |||||||
| chr17:30160315 | T | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.115-12227T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160315 | |||||||
| chr17:30160344 | T | G | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-12198T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160344 | |||||||
| chr17:30160699 | G | A | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-11843G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160699 | |||||||
| chr17:30160884 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.115-11658C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160884 | |||||||
| chr17:30160917 | C | T | 2 | a0001c0002t0001g0063 a0001c0002t0001g0146 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.115-11625C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160917 | |||||||
| chr17:30160958 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-11584C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30160958 | |||||||
| chr17:30161218 | A | C | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-11324A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161218 | |||||||
| chr17:30161383 | T | C | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-11159T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161383 | |||||||
| chr17:30161439 | A | G | 1 | a0001c0002t0001g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.115-11103A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161439 | |||||||
| chr17:30161773 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.115-10769C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30161773 | |||||||
| chr17:30162024 | CT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(166): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.115-10503delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30162024 | ||||||
| chr17:30162082 | C | T | 1 | a0009c0017t0003g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.115-10460C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162082 | |||||||
| chr17:30162086 | G | T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-10456G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162086 | |||||||
| chr17:30162149 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115-10393C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162149 | |||||||
| chr17:30162652 | A | G | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.115-9890A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162652 | |||||||
| chr17:30162752 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-9790G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162752 | |||||||
| chr17:30162758 | A | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.115-9784A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162758 | |||||||
| chr17:30162790 | A | G | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-9752A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30162790 | |||||||
| chr17:30163073 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.115-9469C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163073 | |||||||
| chr17:30163149 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-9393C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163149 | |||||||
| chr17:30163188 | TTTGTGTG others(10): Show |
T | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115-9352_115-9336d others(19): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163188 | ||||||
| chr17:30163189 | T | TTG | 22 | a0001c0001t0001g0160 a0001c0001t0005g0155 a0001c0002t0001g0003 others(19): Show |
22 | HG00609.hp1 HG01167.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-9295_115-9294d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | T | TTGTG | 13 | a0001c0001t0001g0158 a0001c0002t0001g0008 a0001c0002t0001g0041 others(10): Show |
13 | HG00642.hp2 HG01346.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.115-9297_115-9294d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | T | TTGTGTG | 6 | a0001c0001t0005g0154 a0001c0002t0001g0012 a0001c0002t0001g0050 others(3): Show |
6 | HG03195.hp1 HG03209.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-9299_115-9294d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | T | TTGTGTGT others(1): Show |
3 | a0001c0002t0001g0014 a0001c0002t0001g0142 a0003c0005t0001g0265 |
3 | HG00597.hp1 HG02895.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.115-9301_115-9294d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | T | TTGTGTGT others(3): Show |
3 | a0001c0002t0001g0123 a0001c0002t0007g0112 a0003c0005t0001g0266 |
3 | HG06807.hp1 NA18906.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.115-9303_115-9294d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTG | T | 17 | a0001c0001t0001g0132 a0001c0001t0005g0157 a0001c0002t0001g0044 others(14): Show |
17 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.115-9295_115-9294d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTG | T | 19 | a0001c0001t0001g0133 a0001c0002t0001g0019 a0001c0002t0001g0021 others(16): Show |
19 | HG00323.hp2 HG01099.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.115-9297_115-9294d others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTG | T | 16 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0151 others(13): Show |
16 | HG00140.hp2 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-9299_115-9294d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(12): Show |
15 | HG01516.hp2 HG01517.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.115-9301_115-9294d others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0131 a0001c0001t0002g0170 a0001c0001t0002g0176 others(6): Show |
9 | HG00741.hp2 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.115-9303_115-9294d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(5): Show |
T | 8 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0181 others(5): Show |
8 | HG00733.hp2 HG02723.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-9305_115-9294d others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(7): Show |
T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0172 a0001c0001t0002g0246 others(11): Show |
14 | HG00099.hp2 HG00597.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-9307_115-9294d others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(9): Show |
T | 20 | a0001c0001t0002g0084 a0001c0001t0002g0179 a0001c0001t0002g0194 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.115-9309_115-9294d others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(11): Show |
T | 66 | a0001c0001t0002g0083 a0001c0001t0002g0171 a0001c0001t0002g0177 others(63): Show |
66 | HG00323.hp1 HG00609.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.115-9311_115-9294d others(20): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(13): Show |
T | 5 | a0001c0001t0002g0002 a0001c0001t0002g0186 a0001c0001t0002g0219 others(2): Show |
5 | HG01167.hp2 HG01261.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9313_115-9294d others(22): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(15): Show |
T | 1 | a0001c0011t0002g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.115-9315_115-9294d others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163189 | TTGTGTGT others(21): Show |
T | 5 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9321_115-9294d others(30): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163189 | ||||||
| chr17:30163239 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-9301_115-9292d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163239 | ||||||
| chr17:30163243 | GTGTGTT | G | 4 | a0001c0001t0001g0162 a0001c0001t0001g0169 a0001c0002t0003g0027 others(1): Show |
4 | HG01884.hp1 HG02257.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-9297_115-9292d others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163243 | ||||||
| chr17:30163247 | GTT | G | 3 | a0001c0001t0001g0159 a0001c0002t0003g0034 a0001c0002t0003g0035 |
3 | HG02451.hp1 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.115-9291_115-9290d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163247 | ||||||
| chr17:30163249 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115-9293T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163249 | |||||||
| chr17:30163311 | G | A | 26 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0041 others(23): Show |
26 | HG00140.hp2 HG00733.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-9231G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163311 | |||||||
| chr17:30163328 | C | T | 1 | a0001c0002t0001g0088 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.115-9214C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163328 | |||||||
| chr17:30163541 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.115-9001A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163541 | |||||||
| chr17:30163634 | A | G | 1 | a0001c0002t0003g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.115-8908A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163634 | |||||||
| chr17:30163668 | T | C | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-8874T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163668 | |||||||
| chr17:30163675 | ACCACT | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8866_115-8862d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163675 | |||||||
| chr17:30163679 | C | CT | 83 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0171 others(80): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.115-8841dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | ||||||
| chr17:30163679 | C | CTT | 11 | a0001c0001t0002g0187 a0001c0001t0002g0203 a0001c0001t0002g0228 others(8): Show |
11 | HG00597.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-8842_115-8841d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | ||||||
| chr17:30163679 | CT | C | 16 | a0001c0001t0002g0188 a0001c0001t0002g0278 a0001c0001t0002g0279 others(13): Show |
16 | HG01069.hp1 HG01099.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-8841delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30163679 | ||||||
| chr17:30163681 | T | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8861T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163681 | |||||||
| chr17:30163682 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8860T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163682 | |||||||
| chr17:30163684 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8858T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163684 | |||||||
| chr17:30163685 | T | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8857T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163685 | |||||||
| chr17:30163687 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8855T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163687 | |||||||
| chr17:30163796 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-8746C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163796 | |||||||
| chr17:30163887 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-8655C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163887 | |||||||
| chr17:30163913 | T | C | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-8629T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163913 | |||||||
| chr17:30163966 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-8576A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163966 | |||||||
| chr17:30163975 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-8567C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163975 | |||||||
| chr17:30163982 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-8560G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30163982 | |||||||
| chr17:30164010 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.115-8532A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164010 | |||||||
| chr17:30164011 | A | T | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-8531A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164011 | |||||||
| chr17:30164020 | TGTGTGTG others(3): Show |
T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-8514_115-8505d others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30164020 | ||||||
| chr17:30164030 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.115-8512C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164030 | |||||||
| chr17:30164210 | T | C | 1 | a0001c0001t0004g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-8332T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164210 | |||||||
| chr17:30164383 | C | G | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-8159C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164383 | |||||||
| chr17:30164439 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-8103G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164439 | |||||||
| chr17:30164449 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115-8093G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30164449 | |||||||
| chr17:30165015 | C | T | 2 | a0001c0001t0006g0227 a0001c0001t0006g0229 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.115-7527C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165015 | |||||||
| chr17:30165124 | T | C | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-7418T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165124 | |||||||
| chr17:30165293 | A | T | 1 | a0001c0001t0002g0258 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-7249A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165293 | |||||||
| chr17:30165311 | G | C | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115-7231G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165311 | |||||||
| chr17:30165333 | A | T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-7209A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165333 | |||||||
| chr17:30165787 | C | T | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-6755C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165787 | |||||||
| chr17:30165886 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-6656A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165886 | |||||||
| chr17:30165912 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.115-6630A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30165912 | |||||||
| chr17:30166217 | T | G | 1 | a0001c0001t0002g0258 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-6325T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166217 | |||||||
| chr17:30166382 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-6160G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166382 | |||||||
| chr17:30166503 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-6039A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166503 | |||||||
| chr17:30166520 | A | T | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-6022A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166520 | |||||||
| chr17:30166563 | A | T | 1 | a0001c0001t0002g0258 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.115-5979A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166563 | |||||||
| chr17:30166787 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0131 others(131): Show |
136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.115-5755A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166787 | |||||||
| chr17:30166814 | T | C | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5728T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166814 | |||||||
| chr17:30166843 | T | G | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-5699T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166843 | |||||||
| chr17:30166911 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.115-5631G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166911 | |||||||
| chr17:30166985 | A | G | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5557A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30166985 | |||||||
| chr17:30167132 | A | G | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.115-5410A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167132 | |||||||
| chr17:30167135 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-5407C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167135 | |||||||
| chr17:30167164 | T | G | 3 | a0001c0001t0005g0154 a0001c0001t0005g0155 a0001c0001t0005g0157 |
3 | HG02922.hp2 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.115-5378T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167164 | |||||||
| chr17:30167168 | C | T | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.115-5374C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167168 | |||||||
| chr17:30167294 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.115-5248C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167294 | |||||||
| chr17:30167469 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.115-5073C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167469 | |||||||
| chr17:30167611 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-4931A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167611 | |||||||
| chr17:30167664 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.115-4878C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167664 | |||||||
| chr17:30167746 | G | A | 1 | a0001c0002t0001g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.115-4796G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167746 | |||||||
| chr17:30167836 | TA | T | 5 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0218 others(2): Show |
5 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-4704delA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30167836 | ||||||
| chr17:30167841 | A | C | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-4701A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167841 | |||||||
| chr17:30167975 | T | C | 1 | a0001c0002t0003g0039 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-4567T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30167975 | |||||||
| chr17:30168003 | G | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-4539G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168003 | |||||||
| chr17:30168048 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-4494G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168048 | |||||||
| chr17:30168068 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(24): Show |
28 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.115-4474G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168068 | |||||||
| chr17:30168094 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.115-4448A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168094 | |||||||
| chr17:30168428 | A | T | 1 | a0001c0002t0001g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.115-4114A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168428 | |||||||
| chr17:30168537 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.115-4005A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168537 | |||||||
| chr17:30168574 | T | TATA | 14 | a0001c0001t0002g0002 a0001c0001t0002g0228 a0001c0001t0002g0230 others(11): Show |
15 | HG00099.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-3952_115-3950d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168574 | ||||||
| chr17:30168590 | ATAG | A | 3 | a0001c0002t0003g0027 a0001c0002t0003g0034 a0001c0002t0003g0035 |
3 | HG02257.hp2 HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.115-3949_115-3947d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168590 | ||||||
| chr17:30168593 | G | GTAA | 6 | a0001c0002t0003g0016 a0001c0002t0003g0038 a0001c0002t0003g0080 others(3): Show |
6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3933_115-3931d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30168593 | ||||||
| chr17:30168622 | A | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-3920A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168622 | |||||||
| chr17:30168654 | T | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.115-3888T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168654 | |||||||
| chr17:30168751 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.115-3791A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168751 | |||||||
| chr17:30168755 | C | A | 3 | a0003c0005t0001g0264 a0003c0005t0001g0265 a0003c0005t0001g0266 |
3 | HG02895.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.115-3787C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168755 | |||||||
| chr17:30168775 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-3767A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168775 | |||||||
| chr17:30168831 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.115-3711G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30168831 | |||||||
| chr17:30169028 | T | A | 1 | a0001c0002t0001g0124 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.115-3514T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169028 | |||||||
| chr17:30169173 | T | A | 2 | a0001c0001t0004g0274 a0001c0001t0004g0277 |
2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.115-3369T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169173 | |||||||
| chr17:30169195 | A | G | 6 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0044 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3347A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169195 | |||||||
| chr17:30169402 | T | C | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-3140T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169402 | |||||||
| chr17:30169412 | A | T | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-3130A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169412 | |||||||
| chr17:30169762 | T | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.115-2780T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169762 | |||||||
| chr17:30169846 | GA | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(6): Show |
10 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-2685delA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30169846 | ||||||
| chr17:30169853 | A | C | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.115-2689A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169853 | |||||||
| chr17:30169989 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-2553A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30169989 | |||||||
| chr17:30170241 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-2301T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170241 | |||||||
| chr17:30170350 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.115-2192G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170350 | |||||||
| chr17:30170390 | C | T | 6 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0044 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-2152C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170390 | |||||||
| chr17:30170530 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.115-2012A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170530 | |||||||
| chr17:30170594 | A | ATTGTGGC others(40): Show |
1 | a0001c0001t0002g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.115-1947_115-1901d others(49): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30170594 | ||||||
| chr17:30170706 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0234 |
2 | HG01070.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.115-1836A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170706 | |||||||
| chr17:30170737 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-1805A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170737 | |||||||
| chr17:30170929 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.115-1613G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30170929 | |||||||
| chr17:30171011 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-1531C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171011 | |||||||
| chr17:30171217 | A | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-1325A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171217 | |||||||
| chr17:30171303 | CT | C | 142 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(139): Show |
143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.115-1219delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171303 | ||||||
| chr17:30171303 | CTT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
11 | HG02055.hp2 HG02615.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-1220_115-1219d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171303 | ||||||
| chr17:30171336 | G | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.115-1206G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171336 | |||||||
| chr17:30171394 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0013 |
2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.115-1148C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171394 | |||||||
| chr17:30171597 | G | A | 1 | a0001c0001t0002g0194 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.115-945G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171597 | |||||||
| chr17:30171609 | A | G | 1 | a0001c0001t0004g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115-933A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171609 | |||||||
| chr17:30171717 | T | G | 1 | a0001c0002t0001g0125 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.115-825T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171717 | |||||||
| chr17:30171807 | C | A | 3 | a0001c0001t0002g0189 a0001c0001t0002g0217 a0001c0001t0002g0257 |
3 | HG00323.hp1 HG01993.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.115-735C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171807 | |||||||
| chr17:30171934 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.115-608T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171934 | |||||||
| chr17:30171934 | T | TCA | 31 | a0001c0001t0001g0153 a0001c0001t0002g0083 a0001c0001t0002g0180 others(28): Show |
31 | HG00140.hp2 HG00733.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.115-570_115-569dup others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | T | TCACA | 8 | a0001c0002t0001g0017 a0001c0002t0001g0091 a0001c0002t0001g0140 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-572_115-569dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | T | TCACACA | 5 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0003g0080 others(2): Show |
5 | HG01346.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-574_115-569dup others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | T | TCACACAC others(1): Show |
3 | a0001c0001t0005g0157 a0001c0002t0001g0139 a0001c0002t0003g0016 |
3 | HG02922.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.115-576_115-569dup others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | T | TCACACAC others(3): Show |
1 | a0001c0002t0003g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.115-578_115-569dup others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | TCA | T | 16 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0159 others(13): Show |
16 | HG01070.hp1 HG01361.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-570_115-569del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171934 | TCACA | T | 5 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(2): Show |
5 | HG01884.hp2 HG02615.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-572_115-569del others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171934 | ||||||
| chr17:30171958 | A | C | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-584A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171958 | |||||||
| chr17:30171960 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-582A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171960 | |||||||
| chr17:30171962 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-580A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171962 | |||||||
| chr17:30171964 | A | T | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.115-578A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171964 | |||||||
| chr17:30171966 | A | T | 2 | a0001c0001t0002g0241 a0001c0002t0001g0136 |
2 | HG02615.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.115-576A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171966 | |||||||
| chr17:30171966 | ACACACAC others(7): Show |
A | 1 | a0001c0008t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-574_115-561del others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171966 | ||||||
| chr17:30171968 | A | C | 1 | a0001c0001t0002g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.115-574A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171968 | |||||||
| chr17:30171968 | A | T | 3 | a0001c0002t0001g0072 a0001c0002t0001g0136 a0001c0011t0002g0191 |
3 | HG02572.hp2 HG02615.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-574A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171968 | |||||||
| chr17:30171970 | A | ACTCCCTC others(5): Show |
2 | a0001c0001t0002g0203 a0001c0001t0002g0252 |
2 | HG01934.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.115-571_115-570ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171970 | ||||||
| chr17:30171970 | A | C | 2 | a0001c0002t0001g0072 a0001c0011t0002g0191 |
2 | HG02572.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-572A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171970 | |||||||
| chr17:30171970 | A | T | 4 | a0001c0001t0001g0161 a0001c0001t0002g0192 a0001c0001t0002g0241 others(1): Show |
4 | HG02615.hp2 HG02809.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-572A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171970 | |||||||
| chr17:30171972 | A | ACACACAC others(3): Show |
1 | a0001c0002t0007g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACAC others(5): Show |
3 | a0001c0002t0001g0074 a0001c0002t0007g0107 a0005c0004t0001g0048 |
3 | HG01070.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACTC others(1): Show |
3 | a0001c0002t0001g0076 a0001c0002t0001g0102 a0001c0002t0001g0141 |
3 | HG00140.hp1 HG02074.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACTC others(3): Show |
2 | a0001c0002t0001g0113 a0005c0004t0001g0049 |
2 | HG01071.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACTC others(5): Show |
1 | a0005c0004t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACTC others(7): Show |
1 | a0001c0002t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACACTC others(9): Show |
2 | a0001c0002t0001g0056 a0001c0002t0001g0085 |
2 | HG00642.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.115-569_115-568ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCC | 11 | a0001c0002t0001g0019 a0001c0002t0001g0022 a0001c0002t0001g0059 others(8): Show |
11 | HG00609.hp1 HG01099.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(1): Show |
6 | a0001c0002t0001g0006 a0001c0002t0001g0071 a0001c0002t0001g0073 others(3): Show |
6 | HG02622.hp2 HG03209.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(3): Show |
2 | a0001c0002t0001g0088 a0003c0005t0001g0266 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.115-569_115-568ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(5): Show |
4 | a0001c0001t0002g0175 a0001c0002t0001g0045 a0001c0002t0001g0057 others(1): Show |
4 | HG00099.hp1 HG00323.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-569_115-568ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(7): Show |
2 | a0001c0002t0001g0044 a0004c0006t0001g0058 |
2 | HG01496.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.115-569_115-568ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(9): Show |
1 | a0001c0002t0001g0068 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(11): Show |
1 | a0001c0001t0002g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(18): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCC others(17): Show |
1 | a0001c0002t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.115-569_115-568ins others(24): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACACTCCT others(8): Show |
1 | a0001c0002t0001g0046 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.115-569_115-568ins others(15): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | ACTCTCCT others(4): Show |
1 | a0001c0002t0001g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.115-567_115-566ins others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0002g0192 |
2 | HG02809.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.115-570A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171972 | |||||||
| chr17:30171972 | A | T | 76 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0002 others(73): Show |
77 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.115-570A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171972 | |||||||
| chr17:30171972 | ACT | A | 3 | a0001c0002t0001g0078 a0001c0002t0001g0117 a0008c0010t0001g0150 |
3 | HG03486.hp1 NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.115-568_115-567del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171972 | ACTCCCT | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(2): Show |
5 | HG01891.hp1 HG01934.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-566_115-561del others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171972 | ||||||
| chr17:30171974 | T | A | 26 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(23): Show |
26 | HG00741.hp2 HG01192.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.115-568T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171974 | |||||||
| chr17:30171974 | T | C | 64 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0002 others(61): Show |
65 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.115-568T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171974 | |||||||
| chr17:30171976 | C | A | 10 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(7): Show |
10 | HG01192.hp1 HG02055.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-566C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171976 | |||||||
| chr17:30171976 | C | CCT | 18 | a0001c0001t0001g0167 a0001c0002t0001g0005 a0001c0002t0001g0013 others(15): Show |
18 | HG00597.hp1 HG01978.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.115-528_115-527dup others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | ||||||
| chr17:30171976 | C | CCTCT | 3 | a0001c0002t0001g0144 a0001c0002t0003g0032 a0001c0002t0003g0034 |
3 | HG02809.hp1 HG02818.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.115-530_115-527dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | ||||||
| chr17:30171976 | C | CCTCTCTC others(3): Show |
1 | a0001c0002t0001g0018 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.115-536_115-527dup others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | ||||||
| chr17:30171976 | C | CCTCTCTC others(5): Show |
1 | a0001c0002t0001g0007 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.115-538_115-527dup others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | ||||||
| chr17:30171976 | C | T | 140 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0166 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.115-566C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171976 | |||||||
| chr17:30171976 | CCT | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0164 others(4): Show |
7 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-528_115-527del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171976 | ||||||
| chr17:30171978 | T | A | 2 | a0001c0001t0001g0135 a0001c0002t0003g0111 |
2 | HG01192.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115-564T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171978 | |||||||
| chr17:30171978 | T | C | 19 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0094 others(16): Show |
19 | HG00741.hp2 HG01243.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.115-564T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171978 | |||||||
| chr17:30171980 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-562T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171980 | |||||||
| chr17:30171980 | T | C | 8 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(5): Show |
8 | HG02055.hp2 HG03139.hp2 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-562T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171980 | |||||||
| chr17:30171982 | T | C | 2 | a0001c0002t0001g0021 a0001c0002t0003g0111 |
2 | HG01192.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.115-560T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171982 | |||||||
| chr17:30171984 | T | C | 1 | a0001c0008t0001g0163 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-558T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30171984 | |||||||
| chr17:30171988 | T | TCTCTCTC others(4): Show |
1 | a0004c0006t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.115-553_115-543dup others(11): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30171988 | ||||||
| chr17:30172012 | T | A | 3 | a0001c0001t0002g0170 a0001c0001t0002g0233 a0001c0011t0002g0191 |
3 | HG02293.hp2 HG03130.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.115-530T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172012 | |||||||
| chr17:30172014 | T | A | 7 | a0001c0001t0002g0170 a0001c0001t0002g0192 a0001c0001t0002g0203 others(4): Show |
7 | HG01934.hp1 HG02293.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.115-528T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172014 | |||||||
| chr17:30172014 | T | TCACA | 8 | a0001c0001t0002g0171 a0001c0001t0002g0177 a0001c0001t0002g0201 others(5): Show |
8 | HG01070.hp1 HG01123.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-527_115-524dup others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCACACA | 4 | a0001c0001t0002g0202 a0001c0001t0002g0246 a0001c0001t0002g0247 others(1): Show |
4 | HG00597.hp2 HG02647.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-524_115-523ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCACA | 8 | a0001c0001t0002g0084 a0001c0001t0002g0206 a0001c0001t0002g0232 others(5): Show |
8 | HG02004.hp2 HG02280.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(6): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCAC others(1): Show |
16 | a0001c0001t0002g0002 a0001c0001t0002g0172 a0001c0001t0002g0181 others(13): Show |
17 | HG00099.hp2 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(8): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCAC others(3): Show |
1 | a0001c0001t0002g0196 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115-527_115-526ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCTC others(3): Show |
27 | a0001c0001t0002g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(24): Show |
27 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(10): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCTC others(5): Show |
1 | a0001c0001t0002g0183 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.115-527_115-526ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCTC others(5): Show |
14 | a0001c0001t0002g0083 a0001c0001t0002g0194 a0001c0001t0002g0195 others(11): Show |
14 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(12): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCTC others(7): Show |
6 | a0001c0001t0002g0184 a0001c0001t0002g0211 a0001c0001t0002g0216 others(3): Show |
6 | HG00609.hp2 HG01952.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-527_115-526ins others(14): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172014 | T | TCTCTCTC others(9): Show |
1 | a0001c0001t0002g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.115-527_115-526ins others(16): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | 30172014 | ||||||
| chr17:30172265 | A | G | 1 | a0008c0010t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-277A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172265 | |||||||
| chr17:30172386 | T | C | 4 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0218 others(1): Show |
4 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-156T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172386 | |||||||
| chr17:30172456 | C | T | 1 | a0011c0013t0002g0205 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.115-86C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172456 | |||||||
| chr17:30172481 | T | A | 20 | a0001c0002t0001g0022 a0001c0002t0001g0096 a0001c0002t0001g0097 others(17): Show |
20 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.115-61T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172481 | |||||||
| chr17:30172522 | A | G | 1 | a0001c0002t0007g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115-20A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 2/6 | chr17 | 30172522 | |||||||
| chr17:30173195 | C | T | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+597C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173195 | |||||||
| chr17:30173206 | C | T | 4 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0002g0218 others(1): Show |
4 | HG01255.hp1 HG01934.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+608C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173206 | |||||||
| chr17:30173229 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.171+631G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173229 | |||||||
| chr17:30173281 | C | T | 15 | a0001c0002t0003g0016 a0001c0002t0003g0028 a0001c0002t0003g0029 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+683C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173281 | |||||||
| chr17:30173337 | T | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.171+739T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173337 | |||||||
| chr17:30173388 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.171+790C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173388 | |||||||
| chr17:30173439 | T | G | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.171+841T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173439 | |||||||
| chr17:30173447 | A | G | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.171+849A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173447 | |||||||
| chr17:30173463 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+865T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30173463 | |||||||
| chr17:30173532 | ATTAT | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+939_171+942del others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30173532 | ||||||
| chr17:30174053 | T | G | 3 | a0001c0002t0001g0114 a0001c0002t0001g0123 a0001c0002t0001g0125 |
3 | NA18951.hp1 NA18972.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.171+1455T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174053 | |||||||
| chr17:30174088 | A | G | 3 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 |
3 | HG01884.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.171+1490A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174088 | |||||||
| chr17:30174392 | C | G | 1 | a0004c0006t0001g0058 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.171+1794C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174392 | |||||||
| chr17:30174606 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.171+2008A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174606 | |||||||
| chr17:30174660 | T | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.171+2062T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174660 | |||||||
| chr17:30174757 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.171+2159T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174757 | |||||||
| chr17:30174792 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.171+2194G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174792 | |||||||
| chr17:30174797 | T | A | 1 | a0004c0006t0001g0043 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.171+2199T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30174797 | |||||||
| chr17:30175012 | A | G | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171+2414A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175012 | |||||||
| chr17:30175022 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.171+2424A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175022 | |||||||
| chr17:30175200 | C | G | 1 | a0001c0001t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.171+2602C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175200 | |||||||
| chr17:30175349 | C | G | 1 | a0001c0002t0001g0017 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.172-2722C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175349 | |||||||
| chr17:30175624 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2447C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175624 | |||||||
| chr17:30175633 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2438C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175633 | |||||||
| chr17:30175950 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0235 |
3 | HG01496.hp1 HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.172-2121C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30175950 | |||||||
| chr17:30176000 | ACC | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-2062_172-2061d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176000 | ||||||
| chr17:30176092 | T | A | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-1979T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176092 | |||||||
| chr17:30176092 | T | G | 1 | a0001c0002t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.172-1979T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176092 | |||||||
| chr17:30176095 | G | T | 2 | a0001c0002t0001g0114 a0003c0005t0001g0264 |
2 | NA18972.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.172-1976G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176095 | |||||||
| chr17:30176104 | GTTGTT | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(163): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.172-1942_172-1938d others(7): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176104 | ||||||
| chr17:30176181 | G | A | 8 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0131 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-1890G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176181 | |||||||
| chr17:30176351 | A | G | 1 | a0001c0001t0002g0190 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.172-1720A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176351 | |||||||
| chr17:30176525 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.172-1546G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176525 | |||||||
| chr17:30176606 | T | TC | 18 | a0001c0002t0001g0013 a0001c0002t0001g0025 a0001c0002t0001g0026 others(15): Show |
18 | HG01192.hp2 HG01346.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.172-1453dupC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176606 | ||||||
| chr17:30176606 | TC | T | 24 | a0001c0001t0001g0167 a0001c0002t0001g0074 a0001c0002t0001g0098 others(21): Show |
24 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.172-1453delC | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176606 | ||||||
| chr17:30176612 | C | G | 3 | a0001c0002t0001g0076 a0001c0002t0001g0077 a0001c0002t0001g0142 |
3 | HG03942.hp1 HG04115.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.172-1459C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176612 | |||||||
| chr17:30176613 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172-1458C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176613 | |||||||
| chr17:30176618 | C | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0147 a0001c0001t0001g0148 others(27): Show |
31 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.172-1453C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176618 | |||||||
| chr17:30176618 | C | CA | 80 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.172-1443dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30176618 | ||||||
| chr17:30176618 | C | CCA | 27 | a0001c0001t0001g0122 a0001c0001t0002g0170 a0001c0001t0002g0171 others(24): Show |
27 | HG00597.hp2 HG00609.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.172-1453_172-1452i others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176618 | |||||||
| chr17:30176619 | A | C | 1 | a0001c0002t0001g0012 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.172-1452A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176619 | |||||||
| chr17:30176745 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.172-1326C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30176745 | |||||||
| chr17:30177198 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | HG03139.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.172-873C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177198 | |||||||
| chr17:30177298 | G | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-773G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177298 | |||||||
| chr17:30177312 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.172-759C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177312 | |||||||
| chr17:30177371 | G | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-700G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177371 | |||||||
| chr17:30177375 | T | TA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(130): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.172-682dupA | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 30177375 | ||||||
| chr17:30177410 | A | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0226 |
2 | NA18969.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.172-661A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177410 | |||||||
| chr17:30177436 | A | G | 9 | a0001c0002t0003g0028 a0001c0002t0003g0029 a0001c0002t0003g0030 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-635A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177436 | |||||||
| chr17:30177491 | G | C | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.172-580G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177491 | |||||||
| chr17:30177698 | T | C | 1 | a0004c0006t0001g0058 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.172-373T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177698 | |||||||
| chr17:30177745 | T | C | 1 | a0001c0002t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.172-326T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30177745 | |||||||
| chr17:30178002 | A | G | 1 | a0001c0002t0001g0136 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.172-69A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30178002 | |||||||
| chr17:30178006 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(132): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.172-65G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 3/6 | chr17 | 30178006 | |||||||
| chr17:30178278 | A | T | 1 | a0001c0002t0001g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+79A>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178278 | |||||||
| chr17:30178280 | C | A | 1 | a0001c0002t0001g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+81C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178280 | |||||||
| chr17:30178282 | G | C | 1 | a0001c0002t0001g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.300+83G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178282 | |||||||
| chr17:30178374 | T | G | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.300+175T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178374 | |||||||
| chr17:30178465 | A | G | 3 | a0001c0001t0002g0189 a0001c0001t0002g0217 a0001c0001t0002g0257 |
3 | HG00323.hp1 HG01993.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.300+266A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178465 | |||||||
| chr17:30178878 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.301-212A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30178878 | |||||||
| chr17:30179011 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.301-79A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 4/6 | chr17 | 30179011 | |||||||
| chr17:30180003 | C | A | 104 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(101): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.508+706C>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180003 | |||||||
| chr17:30180045 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.508+748G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180045 | |||||||
| chr17:30180225 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.509-683T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180225 | |||||||
| chr17:30180398 | C | T | 103 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(100): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.509-510C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180398 | |||||||
| chr17:30180489 | A | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-419A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180489 | |||||||
| chr17:30180514 | A | G | 11 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-394A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180514 | |||||||
| chr17:30180569 | G | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(28): Show |
32 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.509-339G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180569 | |||||||
| chr17:30180675 | G | A | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.509-233G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180675 | |||||||
| chr17:30180735 | T | C | 1 | a0001c0002t0001g0142 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.509-173T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180735 | |||||||
| chr17:30180807 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509-101C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180807 | |||||||
| chr17:30180836 | C | T | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-72C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180836 | |||||||
| chr17:30180837 | T | A | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-71T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180837 | |||||||
| chr17:30180839 | T | A | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-69T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180839 | |||||||
| chr17:30180840 | ATGTC | A | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.509-64_509-61delCT others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 30180840 | ||||||
| chr17:30180840 | ATGTCTGT others(22): Show |
A | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-66_509-38delGT others(27): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | 30180840 | ||||||
| chr17:30180870 | T | A | 4 | a0001c0001t0004g0274 a0001c0001t0004g0275 a0001c0001t0004g0276 others(1): Show |
4 | HG01433.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.509-38T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 5/6 | chr17 | 30180870 | |||||||
| chr17:30181027 | G | A | 1 | a0001c0014t0008g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.617+11G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181027 | |||||||
| chr17:30181089 | C | G | 6 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0044 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+73C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181089 | |||||||
| chr17:30181280 | C | G | 1 | a0001c0001t0002g0243 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.617+264C>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181280 | |||||||
| chr17:30181380 | T | G | 26 | a0001c0002t0001g0267 a0001c0002t0001g0268 a0001c0002t0001g0269 others(23): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.617+364T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181380 | |||||||
| chr17:30181398 | CT | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(152): Show |
157 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.617+400delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181398 | ||||||
| chr17:30181398 | CTT | C | 12 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(9): Show |
12 | HG01433.hp1 HG01884.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+399_617+400del others(2): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181398 | ||||||
| chr17:30181405 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.617+389T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181405 | |||||||
| chr17:30181416 | T | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+400T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181416 | |||||||
| chr17:30181438 | G | A | 2 | a0001c0002t0003g0034 a0001c0002t0003g0035 |
2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.617+422G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181438 | |||||||
| chr17:30181478 | C | T | 1 | a0001c0002t0001g0010 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.617+462C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181478 | |||||||
| chr17:30181524 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.617+508G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181524 | |||||||
| chr17:30181597 | G | GT | 94 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.617+593dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181597 | ||||||
| chr17:30181597 | G | T | 1 | a0001c0002t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.617+581G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181597 | |||||||
| chr17:30181597 | GT | G | 7 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0280 others(4): Show |
7 | HG01433.hp1 HG01884.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+593delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30181597 | ||||||
| chr17:30181604 | T | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.617+588T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181604 | |||||||
| chr17:30181605 | T | TG | 3 | a0001c0001t0002g0261 a0006c0007t0002g0173 a0006c0007t0002g0260 |
3 | HG00741.hp1 NA18948.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.617+589_617+590ins others(1): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181605 | |||||||
| chr17:30181607 | T | G | 1 | a0001c0002t0003g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617+591T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181607 | |||||||
| chr17:30181610 | G | T | 1 | a0001c0002t0001g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.617+594G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181610 | |||||||
| chr17:30181616 | T | G | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.617+600T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181616 | |||||||
| chr17:30181721 | G | A | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.617+705G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181721 | |||||||
| chr17:30181842 | T | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+826T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181842 | |||||||
| chr17:30181890 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(135): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.617+874A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181890 | |||||||
| chr17:30181901 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0176 |
3 | HG02258.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.617+885C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30181901 | |||||||
| chr17:30182048 | C | CT | 15 | a0001c0002t0001g0022 a0001c0002t0001g0096 a0001c0002t0001g0097 others(12): Show |
15 | HG00609.hp1 HG00639.hp1 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.617+1056dupT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | ||||||
| chr17:30182048 | CT | C | 87 | a0001c0001t0002g0170 a0001c0001t0002g0219 a0001c0001t0002g0228 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.617+1056delT | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | ||||||
| chr17:30182048 | CTT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0130 others(112): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.617+1055_617+1056d others(4): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | ||||||
| chr17:30182048 | CTTT | C | 16 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.617+1054_617+1056d others(5): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 30182048 | ||||||
| chr17:30182072 | T | A | 1 | a0002c0003t0001g0052 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617+1056T>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182072 | |||||||
| chr17:30182584 | G | T | 97 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(94): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.617+1568G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182584 | |||||||
| chr17:30182599 | G | A | 2 | a0001c0002t0001g0023 a0001c0002t0001g0050 |
2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.617+1583G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182599 | |||||||
| chr17:30182646 | A | C | 6 | a0001c0002t0003g0016 a0001c0002t0003g0038 a0001c0002t0003g0080 others(3): Show |
6 | HG01192.hp1 HG01346.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+1630A>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182646 | |||||||
| chr17:30182795 | G | A | 3 | a0001c0001t0002g0180 a0001c0001t0002g0204 a0001c0002t0001g0054 |
3 | HG01261.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.617+1779G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182795 | |||||||
| chr17:30182987 | T | G | 2 | a0001c0001t0002g0278 a0001c0001t0002g0279 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.618-1628T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30182987 | |||||||
| chr17:30183017 | C | T | 2 | a0001c0001t0002g0254 a0001c0001t0002g0255 |
2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.618-1598C>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183017 | |||||||
| chr17:30183087 | G | C | 1 | a0001c0002t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.618-1528G>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183087 | |||||||
| chr17:30183135 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.618-1480G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183135 | |||||||
| chr17:30183231 | A | AG | 93 | a0001c0001t0002g0002 a0001c0001t0002g0083 a0001c0001t0002g0084 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.618-1384_618-1383i others(3): Show |
NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183231 | |||||||
| chr17:30183320 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.618-1295G>A | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183320 | |||||||
| chr17:30183356 | G | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
9 | HG02055.hp2 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.618-1259G>T | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183356 | |||||||
| chr17:30183462 | A | G | 2 | a0001c0002t0001g0023 a0001c0002t0001g0050 |
2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.618-1153A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183462 | |||||||
| chr17:30183638 | T | G | 1 | a0001c0001t0002g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.618-977T>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183638 | |||||||
| chr17:30183990 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.618-625T>C | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30183990 | |||||||
| chr17:30184495 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.618-120A>G | NSRP1 | ENSG00000126653.18 | transcript | ENST00000247026.10 | protein_coding | 6/6 | chr17 | 30184495 |