Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7827 |
| ensemblid | ENSG00000116218.13 |
| hgncid | 13394 |
| symbol | NPHS2 |
| name | NPHS2 stomatin family member, podocin |
| refseq_nuc | NM_014625.4 |
| refseq_prot | NP_055440.1 |
| ensembl_nuc | ENST00000367615.9 |
| ensembl_prot | ENSP00000356587.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 179550539 |
| end | 179575948 |
| strand | - |
| ver | v1.2 |
| region | chr1:179550539-179575948 |
| region5000 | chr1:179545539-179580948 |
| regionname0 | NPHS2_chr1_179550539_179575948 |
| regionname5000 | NPHS2_chr1_179545539_179580948 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 383 | 408 | 84 | 74 | 187 | 17 | 44 | 146 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0002 | 0/0 | 383 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0003 | 0/0 | 383 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0004 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0005 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0006 | 0/0 | 383 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| a0007 | 0/0 | 383 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | MERRA others(378): Show |
chr1 | 179545539 | 179580948 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1149 | 225 | 46 | 46 | 95 | 10 | 27 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0001c0002 | 0/0 | 1149 | 127 | 17 | 21 | 68 | 5 | 16 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0001c0003 | 0/0 | 1149 | 28 | 7 | 4 | 15 | 2 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0001c0004 | 1/0 | 1149 | 23 | 10 | 2 | 9 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0001c0006 | 0/0 | 1149 | 5 | 4 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0002c0005 | 0/0 | 1149 | 11 | 9 | 2 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0003c0008 | 0/0 | 1149 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0004c0011 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0005c0007 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0006c0010 | 0/0 | 1149 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 | ||
| a0007c0009 | 0/0 | 1149 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | ATGGA others(1144): Show |
chr1 | 179545539 | 179580948 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1870 | 117 | 4 | 20 | 67 | 6 | 20 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0001t0003 | 0/1 | 1870 | 59 | 4 | 18 | 26 | 4 | 6 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0001t0006 | 0/0 | 1870 | 29 | 27 | 2 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0001t0007 | 0/0 | 1870 | 16 | 10 | 5 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0001t0008 | 0/0 | 1870 | 3 | 1 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0001t0011 | 0/0 | 1870 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0002t0002 | 0/0 | 1870 | 93 | 3 | 12 | 62 | 4 | 12 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0002t0004 | 0/0 | 1870 | 14 | 8 | 2 | 4 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0002t0005 | 0/0 | 1870 | 15 | 1 | 7 | 2 | 1 | 4 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0002t0009 | 0/0 | 1870 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0002t0010 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0003t0004 | 0/0 | 1870 | 28 | 7 | 4 | 15 | 2 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0004t0005 | 1/0 | 1870 | 23 | 10 | 2 | 9 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0006t0001 | 0/0 | 1870 | 3 | 2 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0001c0006t0007 | 0/0 | 1870 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0002c0005t0003 | 0/0 | 1870 | 11 | 9 | 2 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0003c0008t0003 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0004c0011t0012 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0005c0007t0006 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0006c0010t0006 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| a0007c0009t0001 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | GACCC others(1865): Show |
chr1 | 179545539 | 179580948 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 33 | 0 | 2 | 29 | 0 | 2 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0003 | 0/0 | 18 | 1 | 5 | 6 | 3 | 3 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0004 | 0/0 | 15 | 0 | 8 | 7 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0006 | 0/0 | 13 | 0 | 1 | 9 | 1 | 2 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0010 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0005 | 0/0 | 14 | 13 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0012 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0001t0011g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0001 | 0/0 | 64 | 1 | 7 | 45 | 4 | 7 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0023 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0009 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0009g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0002t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0008 | 0/0 | 12 | 4 | 1 | 6 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0003t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0007 | 0/0 | 12 | 2 | 0 | 9 | 0 | 1 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0004t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0006t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0006t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0001c0006t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0030 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0002c0005t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0003c0008t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0004c0011t0012g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0005c0007t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0006c0010t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| a0007c0009t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00140 | hp1 | a0001 | c0002 | t0005 | g0009 | EUR | GBR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00140 | hp2 | a0001 | c0003 | t0004 | g0008 | EUR | GBR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | FIN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | FIN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0140 | EUR | FIN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00408 | hp2 | a0001 | c0003 | t0004 | g0065 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00423 | hp2 | a0001 | c0004 | t0005 | g0007 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00544 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0131 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00558 | hp2 | a0001 | c0002 | t0004 | g0061 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00597 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00639 | hp2 | a0001 | c0003 | t0004 | g0024 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | CHS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00733 | hp1 | a0001 | c0003 | t0004 | g0008 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0080 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01069 | hp1 | a0001 | c0004 | t0005 | g0055 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01069 | hp2 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01070 | hp1 | a0002 | c0005 | t0003 | g0149 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01071 | hp1 | a0002 | c0005 | t0003 | g0030 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01071 | hp2 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0098 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0018 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0033 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01168 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01175 | hp1 | a0001 | c0003 | t0004 | g0066 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0089 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01192 | hp1 | a0001 | c0004 | t0005 | g0048 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0021 | AMR | PUR | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01256 | hp2 | a0001 | c0002 | t0005 | g0040 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0040 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01433 | hp1 | a0001 | c0003 | t0004 | g0024 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01515 | hp1 | a0001 | c0003 | t0004 | g0024 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01516 | hp2 | a0003 | c0008 | t0003 | g0135 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0090 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02027 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0026 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02132 | hp2 | a0001 | c0003 | t0004 | g0069 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02145 | hp1 | a0004 | c0011 | t0012 | g0128 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02155 | hp2 | a0001 | c0003 | t0004 | g0008 | EAS | CDX | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | CDX | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02451 | hp2 | a0001 | c0004 | t0005 | g0052 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0130 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02615 | hp1 | a0001 | c0004 | t0005 | g0007 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02615 | hp2 | a0005 | c0007 | t0006 | g0153 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02622 | hp2 | a0002 | c0005 | t0003 | g0150 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02630 | hp2 | a0002 | c0005 | t0003 | g0046 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02647 | hp2 | a0001 | c0002 | t0010 | g0161 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02698 | hp1 | a0001 | c0002 | t0005 | g0114 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0087 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02717 | hp1 | a0002 | c0005 | t0003 | g0028 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02717 | hp2 | a0002 | c0005 | t0003 | g0148 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02723 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02738 | hp2 | a0001 | c0002 | t0005 | g0092 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02809 | hp1 | a0002 | c0005 | t0003 | g0028 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0074 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02886 | hp2 | a0002 | c0005 | t0003 | g0028 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02895 | hp1 | a0001 | c0006 | t0007 | g0051 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02896 | hp2 | a0001 | c0004 | t0005 | g0031 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02897 | hp2 | a0001 | c0004 | t0005 | g0031 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02922 | hp1 | a0002 | c0005 | t0003 | g0030 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02970 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03195 | hp1 | a0001 | c0004 | t0005 | g0020 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0064 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03225 | hp1 | a0002 | c0005 | t0003 | g0030 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0020 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03516 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03516 | hp2 | a0001 | c0004 | t0005 | g0020 | AFR | ESN | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0021 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | GWD | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0091 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03669 | hp1 | a0001 | c0004 | t0005 | g0007 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03927 | hp1 | a0001 | c0002 | t0005 | g0009 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0121 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0081 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0009 | SAS | STU | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18522 | hp1 | a0001 | c0002 | t0010 | g0162 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18522 | hp2 | a0001 | c0004 | t0005 | g0007 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | CHB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18747 | hp2 | a0007 | c0009 | t0001 | g0111 | EAS | CHB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18942 | hp1 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18942 | hp2 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18943 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18947 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18950 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18951 | hp1 | a0001 | c0003 | t0004 | g0068 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18957 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18966 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18975 | hp1 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18982 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19000 | hp2 | a0001 | c0003 | t0004 | g0067 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19004 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19006 | hp2 | a0001 | c0003 | t0004 | g0016 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19030 | hp2 | a0001 | c0006 | t0007 | g0049 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19043 | hp1 | a0001 | c0004 | t0005 | g0050 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19043 | hp2 | a0002 | c0005 | t0003 | g0046 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19064 | hp1 | a0001 | c0003 | t0004 | g0008 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19064 | hp2 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19076 | hp2 | a0001 | c0003 | t0004 | g0063 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19077 | hp1 | a0001 | c0002 | t0004 | g0062 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19081 | hp1 | a0001 | c0002 | t0005 | g0043 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19085 | hp1 | a0001 | c0004 | t0005 | g0007 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19087 | hp1 | a0001 | c0002 | t0005 | g0043 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19089 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19090 | hp2 | a0001 | c0002 | t0004 | g0023 | EAS | JPT | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0033 | AFR | YRI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | ASW | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ASW | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0045 | EUR | TSI | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02109 | hp1 | a0001 | c0002 | t0009 | g0026 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0026 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03471 | hp1 | a0006 | c0010 | t0006 | g0158 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG06807 | hp1 | a0001 | c0004 | t0005 | g0053 | AFR | USA | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| HG06807 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | USA | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0129 | AFR | USA | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0075 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0133 | REF | REF | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0005 | g0054 | REF | REF | NPHS2_chr1_179545539_179580948 | NPHS2 | chr1 | 179545539 | 179580948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179552616 | T | C | 1 | a0007 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.860A>G | p.Gln287Arg | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/8 | 944/1870 | 860/1152 | 287/383 | chr1 | 179552616 | |||
| chr1:179557040 | G | A | 1 | a0002 | 11 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(8): Show |
missense_variant | MODERATE | c.725C>T | p.Ala242Val | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/8 | 809/1870 | 725/1152 | 242/383 | chr1 | 179557040 | |||
| chr1:179557079 | C | T | 1 | a0003 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.686G>A | p.Arg229Gln | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/8 | 770/1870 | 686/1152 | 229/383 | chr1 | 179557079 | |||
| chr1:179564737 | G | A | 1 | a0006 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.331C>T | p.Leu111Phe | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/8 | 415/1870 | 331/1152 | 111/383 | chr1 | 179564737 | |||
| chr1:179575683 | G | A | 1 | a0004 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.182C>T | p.Ala61Val | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/8 | 266/1870 | 182/1152 | 61/383 | chr1 | 179575683 | |||
| chr1:179575741 | C | T | 1 | a0005 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.124G>A | p.Gly42Arg | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/8 | 208/1870 | 124/1152 | 42/383 | chr1 | 179575741 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179551287 | T | C | 1 | a0001c0003 | 28 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
synonymous_variant | LOW | c.1038A>G | p.Leu346Leu | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 1122/1870 | 1038/1152 | 346/383 | chr1 | 179551287 | |||
| chr1:179551371 | G | A | 8 | a0001c0001 a0001c0006 a0002c0005 others(5): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
synonymous_variant | LOW | c.954C>T | p.Ala318Ala | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 1038/1870 | 954/1152 | 318/383 | chr1 | 179551371 | |||
| chr1:179551434 | C | T | 1 | a0004c0011 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.891G>A | p.Ala297Ala | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 975/1870 | 891/1152 | 297/383 | chr1 | 179551434 | |||
| chr1:179564780 | G | A | 1 | a0001c0003 | 28 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
synonymous_variant | LOW | c.288C>T | p.Ser96Ser | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/8 | 372/1870 | 288/1152 | 96/383 | chr1 | 179564780 | |||
| chr1:179575763 | T | C | 9 | a0001c0001 a0001c0002 a0001c0003 others(6): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
synonymous_variant | LOW | c.102A>G | p.Gly34Gly | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/8 | 186/1870 | 102/1152 | 34/383 | chr1 | 179575763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179550736 | C | A | 1 | a0004c0011t0012 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*437G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 437 | chr1 | 179550736 | ||||||
| chr1:179550745 | T | C | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(14): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*428A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 428 | chr1 | 179550745 | ||||||
| chr1:179550915 | T | C | 5 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(2): Show |
125 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*258A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 258 | chr1 | 179550915 | ||||||
| chr1:179550973 | C | T | 1 | a0001c0002t0002 | 93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*200G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 200 | chr1 | 179550973 | ||||||
| chr1:179551000 | C | T | 1 | a0001c0001t0011 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 173 | chr1 | 179551000 | ||||||
| chr1:179551016 | C | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(14): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*157G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 157 | chr1 | 179551016 | ||||||
| chr1:179551119 | C | G | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(11): Show |
245 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*54G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 8/8 | 54 | chr1 | 179551119 | ||||||
| chr1:179575915 | C | A | 5 | a0001c0001t0003 a0001c0001t0008 a0001c0002t0009 others(2): Show |
76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-51G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/8 | chr1 | 179575915 | |||||||
| chr1:179575916 | G | C | 4 | a0001c0001t0006 a0001c0002t0010 a0005c0007t0006 others(1): Show |
33 | HG01346.hp1 HG02004.hp1 HG02055.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-52C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/8 | 52 | chr1 | 179575916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:179551525 | C | G | 10 | a0001c0003t0004g0008 a0001c0003t0004g0016 a0001c0003t0004g0022 others(7): Show |
28 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.874-74G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551525 | |||||||
| chr1:179551580 | T | C | 7 | a0001c0001t0006g0154 a0002c0005t0003g0028 a0002c0005t0003g0030 others(4): Show |
12 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.874-129A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551580 | |||||||
| chr1:179551656 | G | A | 7 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(4): Show |
8 | HG02145.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-205C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551656 | |||||||
| chr1:179551709 | G | A | 22 | a0001c0002t0002g0001 a0001c0002t0002g0017 a0001c0002t0002g0035 others(19): Show |
92 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.874-258C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551709 | |||||||
| chr1:179551858 | A | G | 1 | a0001c0002t0002g0082 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.874-407T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551858 | |||||||
| chr1:179551961 | A | G | 1 | a0001c0002t0002g0038 | 2 | NA18995.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.874-510T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551961 | |||||||
| chr1:179551968 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.874-517G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179551968 | |||||||
| chr1:179552125 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(380): Show |
intron_variant | MODIFIER | c.873+478G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552125 | |||||||
| chr1:179552244 | G | A | 1 | a0002c0005t0003g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.873+359C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552244 | |||||||
| chr1:179552297 | A | G | 1 | a0001c0002t0002g0037 | 2 | HG00673.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.873+306T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552297 | |||||||
| chr1:179552344 | G | T | 5 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(2): Show |
15 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.873+259C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552344 | |||||||
| chr1:179552377 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.873+226T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552377 | |||||||
| chr1:179552418 | G | A | 1 | a0001c0004t0005g0020 | 3 | HG03195.hp1 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.873+185C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552418 | |||||||
| chr1:179552440 | A | G | 3 | a0001c0003t0004g0016 a0001c0003t0004g0063 a0001c0003t0004g0067 |
6 | NA18942.hp1 NA18950.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.873+163T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552440 | |||||||
| chr1:179552493 | C | G | 1 | a0001c0001t0006g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.873+110G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552493 | |||||||
| chr1:179552549 | T | C | 4 | a0001c0001t0007g0039 a0001c0001t0007g0080 a0001c0001t0007g0089 others(1): Show |
5 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.873+54A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552549 | |||||||
| chr1:179552596 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.873+7A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 7/7 | chr1 | 179552596 | |||||||
| chr1:179552772 | T | G | 1 | a0001c0003t0004g0065 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.795-91A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179552772 | |||||||
| chr1:179552797 | G | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
206 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.795-116C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179552797 | |||||||
| chr1:179552939 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.795-258A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179552939 | |||||||
| chr1:179552947 | C | A | 5 | a0001c0001t0007g0039 a0001c0001t0007g0080 a0001c0001t0007g0089 others(2): Show |
8 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-266G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179552947 | |||||||
| chr1:179552964 | G | A | 2 | a0001c0003t0004g0024 a0001c0003t0004g0066 |
4 | HG00639.hp2 HG01175.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.795-283C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179552964 | |||||||
| chr1:179553086 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
206 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.795-405T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553086 | |||||||
| chr1:179553092 | A | G | 20 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(17): Show |
44 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.795-411T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553092 | |||||||
| chr1:179553205 | C | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.795-524G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553205 | |||||||
| chr1:179553418 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.795-737T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553418 | |||||||
| chr1:179553466 | G | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.795-785C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553466 | |||||||
| chr1:179553660 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.794+816A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553660 | |||||||
| chr1:179553725 | T | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+751A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553725 | |||||||
| chr1:179553794 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.794+682A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553794 | |||||||
| chr1:179553807 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.794+669T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553807 | |||||||
| chr1:179553817 | C | T | 4 | a0001c0001t0007g0039 a0001c0001t0007g0080 a0001c0001t0007g0089 others(1): Show |
5 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+659G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553817 | |||||||
| chr1:179553862 | C | T | 1 | a0001c0002t0009g0026 | 3 | HG02055.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.794+614G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553862 | |||||||
| chr1:179553865 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+611G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553865 | |||||||
| chr1:179553896 | C | T | 23 | a0001c0002t0002g0001 a0001c0002t0002g0017 a0001c0002t0002g0035 others(20): Show |
93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.794+580G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553896 | |||||||
| chr1:179553906 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+570A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553906 | |||||||
| chr1:179553912 | A | AT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
216 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.794+563dupA | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553912 | |||||||
| chr1:179553912 | A | ATT | 8 | a0001c0001t0001g0042 a0001c0001t0001g0110 a0001c0001t0003g0011 others(5): Show |
15 | HG02071.hp1 HG02145.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.794+562_794+563dup others(2): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553912 | |||||||
| chr1:179553937 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0025 others(13): Show |
42 | HG00099.hp1 HG00558.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.794+539C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553937 | |||||||
| chr1:179553955 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.794+521C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179553955 | |||||||
| chr1:179554015 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.794+461G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554015 | |||||||
| chr1:179554017 | A | T | 1 | a0001c0004t0005g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.794+459T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554017 | |||||||
| chr1:179554058 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
243 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.794+418T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554058 | |||||||
| chr1:179554140 | C | G | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.794+336G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554140 | |||||||
| chr1:179554150 | G | A | 5 | a0002c0005t0003g0030 a0002c0005t0003g0046 a0002c0005t0003g0148 others(2): Show |
8 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.794+326C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554150 | |||||||
| chr1:179554162 | C | T | 4 | a0001c0001t0007g0039 a0001c0001t0007g0080 a0001c0001t0007g0089 others(1): Show |
5 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.794+314G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554162 | |||||||
| chr1:179554418 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.794+58T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554418 | |||||||
| chr1:179554436 | C | T | 1 | a0001c0002t0002g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.794+40G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 6/7 | chr1 | 179554436 | |||||||
| chr1:179554743 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.739-212A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179554743 | |||||||
| chr1:179554918 | G | A | 1 | a0001c0001t0008g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.739-387C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179554918 | |||||||
| chr1:179555157 | G | A | 2 | a0002c0005t0003g0030 a0002c0005t0003g0149 |
4 | HG01070.hp1 HG01071.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-626C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555157 | |||||||
| chr1:179555340 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.739-809C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555340 | |||||||
| chr1:179555374 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.739-843A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555374 | |||||||
| chr1:179555497 | A | G | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.739-966T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555497 | |||||||
| chr1:179555515 | T | G | 10 | a0001c0003t0004g0008 a0001c0003t0004g0016 a0001c0003t0004g0022 others(7): Show |
28 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.739-984A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555515 | |||||||
| chr1:179555575 | G | T | 5 | a0002c0005t0003g0030 a0002c0005t0003g0046 a0002c0005t0003g0148 others(2): Show |
8 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-1044C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555575 | |||||||
| chr1:179555613 | C | T | 7 | a0001c0001t0007g0039 a0001c0001t0007g0080 a0001c0001t0007g0089 others(4): Show |
10 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.739-1082G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555613 | |||||||
| chr1:179555709 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.739-1178C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555709 | |||||||
| chr1:179555732 | T | C | 6 | a0002c0005t0003g0028 a0002c0005t0003g0030 a0002c0005t0003g0046 others(3): Show |
11 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.739-1201A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555732 | |||||||
| chr1:179555829 | A | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.738+1198T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555829 | |||||||
| chr1:179555844 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.738+1183G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555844 | |||||||
| chr1:179555900 | C | T | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.738+1127G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555900 | |||||||
| chr1:179555989 | T | C | 20 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(17): Show |
44 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.738+1038A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179555989 | |||||||
| chr1:179556165 | A | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0029 others(16): Show |
41 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.738+862T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556165 | |||||||
| chr1:179556176 | C | T | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.738+851G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556176 | |||||||
| chr1:179556200 | G | T | 2 | a0001c0002t0002g0035 a0001c0002t0002g0076 |
3 | HG01081.hp2 HG03834.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.738+827C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556200 | |||||||
| chr1:179556213 | G | C | 1 | a0001c0002t0002g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.738+814C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556213 | |||||||
| chr1:179556259 | A | T | 1 | a0001c0004t0005g0053 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.738+768T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556259 | |||||||
| chr1:179556398 | A | C | 3 | a0001c0002t0005g0091 a0001c0004t0005g0052 a0001c0004t0005g0055 |
3 | HG01069.hp1 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.738+629T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556398 | |||||||
| chr1:179556425 | C | T | 1 | a0001c0002t0002g0079 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.738+602G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556425 | |||||||
| chr1:179556436 | G | A | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.738+591C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556436 | |||||||
| chr1:179556676 | T | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(3): Show |
16 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.738+351A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556676 | |||||||
| chr1:179556691 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.738+336C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556691 | |||||||
| chr1:179556729 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.738+298G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556729 | |||||||
| chr1:179556917 | A | T | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.738+110T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 5/7 | chr1 | 179556917 | |||||||
| chr1:179557289 | G | T | 1 | a0001c0001t0003g0134 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.535-59C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179557289 | |||||||
| chr1:179557326 | C | T | 2 | a0001c0002t0004g0034 a0001c0002t0004g0064 |
3 | HG02109.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.535-96G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179557326 | |||||||
| chr1:179557327 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0130 |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-97C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179557327 | |||||||
| chr1:179557435 | T | C | 1 | a0002c0005t0003g0046 | 2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.535-205A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179557435 | |||||||
| chr1:179557566 | A | G | 1 | a0001c0004t0005g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.535-336T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179557566 | |||||||
| chr1:179558048 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(101): Show |
249 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.535-818G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558048 | |||||||
| chr1:179558135 | A | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
194 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.535-905T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558135 | |||||||
| chr1:179558151 | G | A | 8 | a0001c0001t0006g0005 a0001c0001t0007g0032 a0001c0001t0007g0058 others(5): Show |
22 | HG01346.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-921C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558151 | |||||||
| chr1:179558189 | A | G | 1 | a0001c0002t0004g0061 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.535-959T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558189 | |||||||
| chr1:179558246 | T | TC | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
246 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.535-1017dupG | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558246 | |||||||
| chr1:179558246 | T | TG | 1 | a0001c0002t0009g0026 | 3 | HG02055.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.535-1017_535-1016i others(3): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558246 | |||||||
| chr1:179558266 | A | G | 24 | a0001c0001t0007g0080 a0001c0002t0002g0001 a0001c0002t0002g0017 others(21): Show |
94 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.535-1036T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558266 | |||||||
| chr1:179558382 | G | C | 1 | a0001c0001t0003g0044 | 2 | NA18977.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.535-1152C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558382 | |||||||
| chr1:179558397 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.535-1167A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558397 | |||||||
| chr1:179558478 | A | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.534+1201T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558478 | |||||||
| chr1:179558843 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.534+836C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558843 | |||||||
| chr1:179558857 | A | G | 11 | a0001c0001t0006g0012 a0001c0001t0006g0047 a0001c0001t0006g0155 others(8): Show |
18 | HG02004.hp1 HG02258.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+822T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558857 | |||||||
| chr1:179558913 | T | C | 1 | a0002c0005t0003g0028 | 3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.534+766A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179558913 | |||||||
| chr1:179559027 | TG | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.534+651delC | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179559027 | |||||||
| chr1:179559295 | A | T | 1 | a0001c0002t0009g0026 | 3 | HG02055.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.534+384T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 4/7 | chr1 | 179559295 | |||||||
| chr1:179559782 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.452-21C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559782 | |||||||
| chr1:179559792 | A | G | 9 | a0001c0001t0006g0005 a0001c0001t0007g0032 a0001c0001t0007g0058 others(6): Show |
23 | HG01346.hp1 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.452-31T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559792 | |||||||
| chr1:179559793 | A | C | 1 | a0001c0001t0007g0060 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.452-32T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559793 | |||||||
| chr1:179559807 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.452-46C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559807 | |||||||
| chr1:179559869 | A | G | 1 | a0001c0002t0002g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.452-108T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559869 | |||||||
| chr1:179559905 | G | A | 4 | a0001c0001t0007g0039 a0001c0001t0007g0089 a0001c0001t0007g0090 others(1): Show |
7 | HG00735.hp2 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-144C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559905 | |||||||
| chr1:179559942 | A | G | 2 | a0001c0001t0006g0005 a0001c0002t0010g0162 |
15 | HG01346.hp1 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.452-181T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179559942 | |||||||
| chr1:179560015 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
288 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.452-254A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560015 | |||||||
| chr1:179560026 | G | A | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.452-265C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560026 | |||||||
| chr1:179560037 | G | A | 1 | a0001c0004t0005g0031 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.452-276C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560037 | |||||||
| chr1:179560152 | T | C | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-391A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560152 | |||||||
| chr1:179560242 | T | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.452-481A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560242 | |||||||
| chr1:179560388 | A | G | 23 | a0001c0001t0006g0005 a0001c0001t0006g0012 a0001c0001t0006g0047 others(20): Show |
47 | HG00735.hp2 HG01109.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.452-627T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560388 | |||||||
| chr1:179560404 | A | G | 1 | a0001c0001t0006g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.452-643T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560404 | |||||||
| chr1:179560413 | T | A | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-652A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560413 | |||||||
| chr1:179560510 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.452-749C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560510 | |||||||
| chr1:179560517 | C | G | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.452-756G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560517 | |||||||
| chr1:179560660 | T | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0146 |
12 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.451+629A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560660 | |||||||
| chr1:179560698 | C | T | 6 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(3): Show |
16 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.451+591G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560698 | |||||||
| chr1:179560799 | G | T | 4 | a0001c0001t0007g0039 a0001c0001t0007g0089 a0001c0001t0007g0090 others(1): Show |
7 | HG00735.hp2 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.451+490C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560799 | |||||||
| chr1:179560879 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.451+410C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560879 | |||||||
| chr1:179560882 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.451+407T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560882 | |||||||
| chr1:179560883 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.451+406G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560883 | |||||||
| chr1:179560918 | A | G | 1 | a0001c0001t0007g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.451+371T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179560918 | |||||||
| chr1:179561006 | A | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.451+283T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179561006 | |||||||
| chr1:179561038 | T | C | 1 | a0001c0001t0003g0138 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.451+251A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179561038 | |||||||
| chr1:179561096 | T | C | 2 | a0001c0002t0002g0017 a0001c0002t0002g0085 |
5 | HG02523.hp1 NA18954.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+193A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179561096 | |||||||
| chr1:179561186 | A | T | 1 | a0001c0004t0005g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.451+103T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 3/7 | chr1 | 179561186 | |||||||
| chr1:179561786 | G | C | 1 | a0001c0002t0005g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.379-425C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179561786 | |||||||
| chr1:179561791 | T | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.379-430A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179561791 | |||||||
| chr1:179561874 | C | T | 1 | a0001c0002t0004g0033 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.379-513G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179561874 | |||||||
| chr1:179561981 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.379-620T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179561981 | |||||||
| chr1:179562192 | A | G | 1 | a0001c0003t0004g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.379-831T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562192 | |||||||
| chr1:179562208 | C | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0108 a0001c0001t0001g0112 others(1): Show |
18 | HG00621.hp1 HG01106.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.379-847G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562208 | |||||||
| chr1:179562230 | G | A | 31 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(28): Show |
102 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.379-869C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562230 | |||||||
| chr1:179562459 | C | T | 68 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(65): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.379-1098G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562459 | |||||||
| chr1:179562473 | G | T | 2 | a0001c0001t0006g0005 a0001c0002t0010g0162 |
15 | HG01346.hp1 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-1112C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562473 | |||||||
| chr1:179562482 | G | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.379-1121C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562482 | |||||||
| chr1:179562543 | A | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.379-1182T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562543 | |||||||
| chr1:179562555 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(377): Show |
intron_variant | MODIFIER | c.379-1194A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562555 | |||||||
| chr1:179562557 | A | C | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.379-1196T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562557 | |||||||
| chr1:179562588 | A | G | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-1227T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562588 | |||||||
| chr1:179562672 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.379-1311A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562672 | |||||||
| chr1:179562767 | A | C | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.379-1406T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562767 | |||||||
| chr1:179562870 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0118 |
4 | HG02040.hp2 HG02135.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-1509G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562870 | |||||||
| chr1:179562941 | A | G | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.379-1580T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562941 | |||||||
| chr1:179562959 | A | G | 1 | a0001c0004t0005g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379-1598T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562959 | |||||||
| chr1:179562960 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(382): Show |
intron_variant | MODIFIER | c.379-1599A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562960 | |||||||
| chr1:179562986 | G | A | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.379-1625C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179562986 | |||||||
| chr1:179563009 | G | A | 1 | a0001c0002t0002g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379-1648C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563009 | |||||||
| chr1:179563013 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.379-1652C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563013 | |||||||
| chr1:179563145 | C | T | 1 | a0001c0002t0009g0026 | 3 | HG02055.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.378+1545G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563145 | |||||||
| chr1:179563163 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.378+1527C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563163 | |||||||
| chr1:179563231 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.378+1459A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563231 | |||||||
| chr1:179563326 | A | C | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.378+1364T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563326 | |||||||
| chr1:179563328 | GA | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.378+1361delT | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563328 | |||||||
| chr1:179563577 | A | G | 1 | a0001c0001t0007g0089 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.378+1113T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563577 | |||||||
| chr1:179563616 | G | A | 66 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(63): Show |
150 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.378+1074C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563616 | |||||||
| chr1:179563653 | A | G | 1 | a0001c0002t0002g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.378+1037T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563653 | |||||||
| chr1:179563940 | G | A | 29 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(26): Show |
67 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.378+750C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179563940 | |||||||
| chr1:179564032 | G | T | 1 | a0001c0002t0002g0017 | 4 | NA18954.hp2 NA18963.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+658C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179564032 | |||||||
| chr1:179564177 | C | T | 27 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(24): Show |
65 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.378+513G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179564177 | |||||||
| chr1:179564220 | T | C | 2 | a0001c0002t0005g0091 a0001c0006t0007g0049 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.378+470A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 2/7 | chr1 | 179564220 | |||||||
| chr1:179564905 | G | T | 1 | a0001c0001t0008g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275-112C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179564905 | |||||||
| chr1:179565117 | A | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-324T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565117 | |||||||
| chr1:179565119 | T | A | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-326A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565119 | |||||||
| chr1:179565123 | A | C | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-330T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565123 | |||||||
| chr1:179565200 | G | A | 1 | a0002c0005t0003g0028 | 3 | HG02717.hp1 HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.275-407C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565200 | |||||||
| chr1:179565209 | C | T | 22 | a0001c0001t0006g0005 a0001c0001t0006g0012 a0001c0001t0006g0047 others(19): Show |
50 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.275-416G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565209 | |||||||
| chr1:179565322 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.275-529G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565322 | |||||||
| chr1:179565375 | C | T | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-582G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565375 | |||||||
| chr1:179565405 | T | G | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.275-612A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565405 | |||||||
| chr1:179565408 | A | G | 1 | a0001c0003t0004g0065 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.275-615T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565408 | |||||||
| chr1:179565431 | T | A | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-638A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565431 | |||||||
| chr1:179565453 | G | T | 1 | a0001c0001t0006g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.275-660C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565453 | |||||||
| chr1:179565640 | T | C | 32 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(29): Show |
103 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.275-847A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565640 | |||||||
| chr1:179565693 | G | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-900C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565693 | |||||||
| chr1:179565702 | C | A | 2 | a0001c0001t0007g0073 a0001c0001t0007g0074 |
2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.275-909G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565702 | |||||||
| chr1:179565815 | T | C | 1 | a0001c0002t0005g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.275-1022A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565815 | |||||||
| chr1:179565817 | T | C | 67 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(64): Show |
151 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.275-1024A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565817 | |||||||
| chr1:179565822 | T | C | 1 | a0001c0002t0002g0087 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.275-1029A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565822 | |||||||
| chr1:179565825 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.275-1032C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565825 | |||||||
| chr1:179565854 | G | A | 1 | a0001c0001t0003g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.275-1061C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179565854 | |||||||
| chr1:179566081 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.275-1288G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566081 | |||||||
| chr1:179566137 | T | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-1344A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566137 | |||||||
| chr1:179566427 | T | A | 1 | a0001c0001t0007g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.275-1634A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566427 | |||||||
| chr1:179566460 | A | T | 5 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0072 others(2): Show |
6 | HG02145.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.275-1667T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566460 | |||||||
| chr1:179566567 | A | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-1774T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566567 | |||||||
| chr1:179566569 | T | A | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.275-1776A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566569 | |||||||
| chr1:179566585 | T | C | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.275-1792A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566585 | |||||||
| chr1:179566824 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.275-2031G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566824 | |||||||
| chr1:179566926 | C | G | 1 | a0001c0006t0007g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.275-2133G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566926 | |||||||
| chr1:179566998 | T | TG | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.275-2206dupC | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179566998 | |||||||
| chr1:179567062 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0130 |
4 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.275-2269A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567062 | |||||||
| chr1:179567071 | A | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-2278T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567071 | |||||||
| chr1:179567241 | T | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-2448A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567241 | |||||||
| chr1:179567541 | A | G | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-2748T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567541 | |||||||
| chr1:179567566 | G | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-2773C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567566 | |||||||
| chr1:179567620 | G | C | 6 | a0001c0001t0006g0012 a0001c0001t0006g0155 a0001c0001t0006g0156 others(3): Show |
12 | HG02004.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.275-2827C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567620 | |||||||
| chr1:179567714 | G | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-2921C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567714 | |||||||
| chr1:179567791 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.275-2998C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567791 | |||||||
| chr1:179567840 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-3047A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567840 | |||||||
| chr1:179567890 | C | T | 1 | a0001c0001t0001g0013 | 5 | HG03490.hp1 HG03492.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-3097G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567890 | |||||||
| chr1:179567925 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-3132G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567925 | |||||||
| chr1:179567982 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.275-3189C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567982 | |||||||
| chr1:179567996 | A | T | 1 | a0001c0001t0003g0132 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.275-3203T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179567996 | |||||||
| chr1:179568053 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0002t0005g0114 |
3 | HG02698.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.275-3260A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568053 | |||||||
| chr1:179568084 | GA | G | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-3292delT | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568084 | |||||||
| chr1:179568123 | G | A | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-3330C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568123 | |||||||
| chr1:179568149 | T | G | 28 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(25): Show |
66 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.275-3356A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568149 | |||||||
| chr1:179568161 | C | T | 6 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(3): Show |
16 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.275-3368G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568161 | |||||||
| chr1:179568203 | G | C | 44 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(41): Show |
104 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.275-3410C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568203 | |||||||
| chr1:179568340 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0124 |
2 | HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.275-3547A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568340 | |||||||
| chr1:179568410 | C | A | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.275-3617G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568410 | |||||||
| chr1:179568575 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-3782A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568575 | |||||||
| chr1:179568579 | T | C | 32 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(29): Show |
103 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.275-3786A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568579 | |||||||
| chr1:179568725 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(379): Show |
intron_variant | MODIFIER | c.275-3932G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568725 | |||||||
| chr1:179568858 | G | A | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-4065C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568858 | |||||||
| chr1:179568882 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-4089C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179568882 | |||||||
| chr1:179569066 | T | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(18): Show |
45 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.275-4273A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569066 | |||||||
| chr1:179569066 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.275-4273A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569066 | |||||||
| chr1:179569150 | G | T | 6 | a0002c0005t0003g0028 a0002c0005t0003g0030 a0002c0005t0003g0046 others(3): Show |
11 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.275-4357C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569150 | |||||||
| chr1:179569242 | G | T | 1 | a0001c0001t0006g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.275-4449C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569242 | |||||||
| chr1:179569277 | G | A | 2 | a0001c0002t0002g0088 a0001c0002t0002g0093 |
2 | NA18974.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.275-4484C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569277 | |||||||
| chr1:179569328 | T | TCTTTGTT others(2): Show |
1 | a0001c0006t0001g0021 | 3 | HG01243.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.275-4536_275-4535i others(11): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569328 | |||||||
| chr1:179569328 | T | TCTTTGTT others(2): Show |
145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(380): Show |
intron_variant | MODIFIER | c.275-4536_275-4535i others(11): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569328 | |||||||
| chr1:179569353 | T | A | 1 | a0001c0001t0007g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.275-4560A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569353 | |||||||
| chr1:179569371 | T | C | 24 | a0001c0001t0007g0080 a0001c0002t0002g0001 a0001c0002t0002g0017 others(21): Show |
94 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.275-4578A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569371 | |||||||
| chr1:179569400 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.275-4607A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569400 | |||||||
| chr1:179569482 | T | G | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.275-4689A>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569482 | |||||||
| chr1:179569496 | A | G | 32 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(29): Show |
103 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.275-4703T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569496 | |||||||
| chr1:179569562 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.275-4769T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569562 | |||||||
| chr1:179569739 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.275-4946C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569739 | |||||||
| chr1:179569800 | G | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG02602.hp1 HG03017.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-5007C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569800 | |||||||
| chr1:179569890 | T | C | 12 | a0001c0001t0006g0005 a0001c0001t0006g0012 a0001c0001t0006g0047 others(9): Show |
32 | HG01346.hp1 HG02004.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.275-5097A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179569890 | |||||||
| chr1:179570077 | T | A | 1 | a0001c0003t0004g0069 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.275-5284A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570077 | |||||||
| chr1:179570100 | A | G | 22 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(19): Show |
46 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.275-5307T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570100 | |||||||
| chr1:179570101 | T | A | 1 | a0001c0004t0005g0055 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.275-5308A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570101 | |||||||
| chr1:179570148 | G | A | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.275-5355C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570148 | |||||||
| chr1:179570212 | T | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.274+5379A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570212 | |||||||
| chr1:179570343 | C | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0047 a0001c0001t0006g0155 others(6): Show |
16 | HG02004.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.274+5248G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570343 | |||||||
| chr1:179570418 | T | TG | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.274+5172dupC | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570418 | |||||||
| chr1:179570484 | C | T | 1 | a0001c0003t0004g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.274+5107G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570484 | |||||||
| chr1:179570495 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274+5096A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570495 | |||||||
| chr1:179570605 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.274+4986T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570605 | |||||||
| chr1:179570716 | G | C | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+4875C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570716 | |||||||
| chr1:179570872 | C | T | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+4719G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570872 | |||||||
| chr1:179570961 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.274+4630C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179570961 | |||||||
| chr1:179571083 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274+4508A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571083 | |||||||
| chr1:179571186 | C | T | 20 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0027 others(17): Show |
44 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.274+4405G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571186 | |||||||
| chr1:179571224 | T | A | 1 | a0001c0001t0003g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.274+4367A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571224 | |||||||
| chr1:179571251 | A | G | 64 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(61): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.274+4340T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571251 | |||||||
| chr1:179571371 | G | A | 20 | a0001c0001t0006g0005 a0001c0001t0006g0012 a0001c0001t0006g0047 others(17): Show |
46 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.274+4220C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571371 | |||||||
| chr1:179571461 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(17): Show |
61 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.274+4130C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571461 | |||||||
| chr1:179571543 | G | T | 2 | a0001c0001t0006g0005 a0001c0002t0010g0162 |
15 | HG01346.hp1 HG02055.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.274+4048C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571543 | |||||||
| chr1:179571587 | C | G | 7 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(4): Show |
17 | HG01106.hp1 HG01433.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.274+4004G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571587 | |||||||
| chr1:179571699 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.274+3892G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571699 | |||||||
| chr1:179571762 | A | T | 1 | a0001c0002t0009g0026 | 3 | HG02055.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.274+3829T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571762 | |||||||
| chr1:179571775 | G | A | 1 | a0001c0001t0006g0047 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.274+3816C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571775 | |||||||
| chr1:179571795 | G | C | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.274+3796C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571795 | |||||||
| chr1:179571803 | G | A | 1 | a0001c0001t0007g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274+3788C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571803 | |||||||
| chr1:179571832 | G | A | 1 | a0001c0002t0002g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.274+3759C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571832 | |||||||
| chr1:179571855 | G | A | 2 | a0001c0001t0006g0159 a0001c0001t0006g0160 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.274+3736C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179571855 | |||||||
| chr1:179572006 | C | T | 4 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0061 others(1): Show |
7 | HG00558.hp2 HG01109.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.274+3585G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572006 | |||||||
| chr1:179572034 | A | G | 1 | a0001c0002t0010g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274+3557T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572034 | |||||||
| chr1:179572040 | T | C | 68 | a0001c0001t0003g0006 a0001c0001t0003g0010 a0001c0001t0003g0011 others(65): Show |
152 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.274+3551A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572040 | |||||||
| chr1:179572082 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.274+3509G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572082 | |||||||
| chr1:179572170 | A | C | 1 | a0001c0002t0002g0070 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.274+3421T>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572170 | |||||||
| chr1:179572172 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.274+3419G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572172 | |||||||
| chr1:179572306 | A | T | 16 | a0001c0001t0006g0005 a0001c0001t0006g0012 a0001c0001t0006g0047 others(13): Show |
39 | HG00735.hp2 HG01109.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.274+3285T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572306 | |||||||
| chr1:179572351 | C | G | 30 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(27): Show |
101 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.274+3240G>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572351 | |||||||
| chr1:179572559 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0122 a0001c0001t0001g0123 others(1): Show |
8 | HG00438.hp2 HG02027.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+3032A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572559 | |||||||
| chr1:179572606 | A | T | 16 | a0001c0002t0004g0023 a0001c0002t0004g0033 a0001c0002t0004g0034 others(13): Show |
38 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.274+2985T>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572606 | |||||||
| chr1:179572725 | G | A | 1 | a0001c0002t0002g0094 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.274+2866C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572725 | |||||||
| chr1:179572804 | C | CTTCT | 3 | a0001c0001t0007g0126 a0001c0001t0007g0127 a0004c0011t0012g0128 |
3 | HG01884.hp2 HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.274+2783_274+2786d others(6): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572804 | |||||||
| chr1:179572977 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.274+2614C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179572977 | |||||||
| chr1:179573235 | A | G | 1 | a0002c0005t0003g0148 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.274+2356T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573235 | |||||||
| chr1:179573351 | G | A | 15 | a0001c0001t0003g0006 a0001c0001t0003g0029 a0001c0001t0003g0044 others(12): Show |
30 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.274+2240C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573351 | |||||||
| chr1:179573358 | T | C | 1 | a0001c0001t0006g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274+2233A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573358 | |||||||
| chr1:179573413 | T | C | 1 | a0001c0001t0008g0143 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.274+2178A>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573413 | |||||||
| chr1:179573414 | C | T | 1 | a0001c0003t0004g0022 | 3 | HG02451.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.274+2177G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573414 | |||||||
| chr1:179573467 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(42): Show |
127 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.274+2124C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573467 | |||||||
| chr1:179573526 | C | T | 1 | a0001c0001t0006g0005 | 14 | HG01346.hp1 HG02055.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.274+2065G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573526 | |||||||
| chr1:179573656 | T | A | 1 | a0001c0001t0008g0143 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.274+1935A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573656 | |||||||
| chr1:179573696 | G | T | 1 | a0001c0001t0008g0143 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.274+1895C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573696 | |||||||
| chr1:179573821 | G | A | 1 | a0001c0002t0004g0018 | 4 | HG01099.hp2 HG02486.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+1770C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573821 | |||||||
| chr1:179573833 | C | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0125 |
2 | HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.274+1758G>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573833 | |||||||
| chr1:179573990 | C | T | 4 | a0001c0001t0007g0032 a0001c0001t0007g0058 a0001c0001t0007g0059 others(1): Show |
5 | HG02809.hp2 HG02976.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+1601G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179573990 | |||||||
| chr1:179574040 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.274+1551C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574040 | |||||||
| chr1:179574263 | A | G | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274+1328T>C | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574263 | |||||||
| chr1:179574283 | G | GATTTTGG others(3): Show |
1 | a0001c0001t0008g0143 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.274+1298_274+1307d others(12): Show |
NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574283 | |||||||
| chr1:179574303 | C | T | 1 | a0001c0001t0006g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.274+1288G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574303 | |||||||
| chr1:179574453 | T | A | 13 | a0001c0001t0003g0011 a0001c0001t0003g0019 a0001c0001t0003g0045 others(10): Show |
28 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.274+1138A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574453 | |||||||
| chr1:179574590 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.274+1001G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574590 | |||||||
| chr1:179574699 | G | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0147 |
4 | HG00323.hp1 HG00733.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.274+892C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574699 | |||||||
| chr1:179574705 | G | T | 5 | a0002c0005t0003g0030 a0002c0005t0003g0046 a0002c0005t0003g0148 others(2): Show |
8 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+886C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179574705 | |||||||
| chr1:179575020 | G | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.274+571C>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575020 | |||||||
| chr1:179575059 | G | A | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274+532C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575059 | |||||||
| chr1:179575119 | G | C | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274+472C>G | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575119 | |||||||
| chr1:179575180 | G | A | 2 | a0001c0001t0007g0126 a0001c0001t0007g0127 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.274+411C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575180 | |||||||
| chr1:179575190 | G | A | 5 | a0002c0005t0003g0030 a0002c0005t0003g0046 a0002c0005t0003g0148 others(2): Show |
8 | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.274+401C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575190 | |||||||
| chr1:179575224 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.274+367G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575224 | |||||||
| chr1:179575245 | T | A | 1 | a0001c0001t0003g0151 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.274+346A>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575245 | |||||||
| chr1:179575394 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.274+197C>T | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575394 | |||||||
| chr1:179575453 | C | T | 1 | a0004c0011t0012g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.274+138G>A | NPHS2 | ENSG00000116218.13 | transcript | ENST00000367615.9 | protein_coding | 1/7 | chr1 | 179575453 |