Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 115677 |
| ensemblid | ENSG00000163072.16 |
| hgncid | 20203 |
| symbol | NOSTRIN |
| name | nitric oxide synthase trafficking |
| refseq_nuc | NM_001039724.4 |
| refseq_prot | NP_001034813.2 |
| ensembl_nuc | ENST00000317647.12 |
| ensembl_prot | ENSP00000318921.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 168802637 |
| end | 168865514 |
| strand | + |
| ver | v1.2 |
| region | chr2:168802637-168865514 |
| region5000 | chr2:168797637-168870514 |
| regionname0 | NOSTRIN_chr2_168802637_168865514 |
| regionname5000 | NOSTRIN_chr2_168797637_168870514 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 506 | 277 | 79 | 48 | 99 | 11 | 39 | 71 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | MRDPL others(501): Show |
chr2 | 168797637 | 168870514 |
| a0002 | 1/0 | 506 | 38 | 3 | 15 | 15 | 3 | 1 | 15 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | MRDPL others(501): Show |
chr2 | 168797637 | 168870514 |
| a0003 | 0/0 | 506 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | MRDPL others(501): Show |
chr2 | 168797637 | 168870514 |
| a0004 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | MRDPL others(501): Show |
chr2 | 168797637 | 168870514 |
| a0005 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | MRDPL others(501): Show |
chr2 | 168797637 | 168870514 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1518 | 151 | 39 | 31 | 53 | 6 | 22 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0002 | 0/0 | 1518 | 49 | 2 | 4 | 35 | 0 | 8 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0004 | 0/1 | 1518 | 32 | 6 | 10 | 5 | 3 | 7 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0005 | 0/0 | 1518 | 29 | 24 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0007 | 0/0 | 1518 | 8 | 0 | 1 | 6 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0008 | 0/0 | 1518 | 3 | 3 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0009 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0010 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0001c0012 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0002c0003 | 1/0 | 1518 | 38 | 3 | 15 | 15 | 3 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0003c0006 | 0/0 | 1518 | 8 | 7 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0003c0013 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0004c0011 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 | ||
| a0005c0014 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ATGAG others(1513): Show |
chr2 | 168797637 | 168870514 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2075 | 122 | 24 | 22 | 52 | 4 | 20 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0001t0002 | 0/0 | 2075 | 26 | 13 | 9 | 0 | 2 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0001t0004 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0001t0005 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0002t0002 | 0/0 | 2075 | 49 | 2 | 4 | 35 | 0 | 8 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0004t0002 | 0/1 | 2075 | 32 | 6 | 10 | 5 | 3 | 7 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0005t0003 | 0/0 | 2075 | 29 | 24 | 2 | 0 | 2 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0007t0001 | 0/0 | 2075 | 7 | 0 | 1 | 6 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0007t0006 | 0/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0008t0003 | 0/0 | 2075 | 3 | 3 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0009t0001 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0010t0001 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0001c0012t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0002c0003t0001 | 1/0 | 2075 | 38 | 3 | 15 | 15 | 3 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0003c0006t0001 | 0/0 | 2075 | 7 | 6 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0003c0006t0002 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0003c0013t0003 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0004c0011t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| a0005c0014t0001 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | ACATT others(2070): Show |
chr2 | 168797637 | 168870514 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0005t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0007t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0008t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0009t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0010t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0010t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0001c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0006t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0003c0013t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0004c0011t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| a0005c0014t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0035 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0269 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00140 | hp1 | a0001 | c0004 | t0002 | g0191 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0045 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00323 | hp2 | a0002 | c0003 | t0001 | g0036 | EUR | FIN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0293 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00673 | hp2 | a0001 | c0004 | t0002 | g0279 | EAS | CHS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00733 | hp2 | a0001 | c0004 | t0002 | g0192 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00735 | hp2 | a0001 | c0004 | t0002 | g0005 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0005 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG00738 | hp2 | a0001 | c0004 | t0002 | g0229 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0018 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01070 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0051 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0247 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01106 | hp2 | a0001 | c0004 | t0002 | g0190 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0038 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0163 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01175 | hp1 | a0001 | c0004 | t0002 | g0268 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0218 | AMR | PUR | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01255 | hp2 | a0001 | c0005 | t0003 | g0236 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0033 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01261 | hp1 | a0001 | c0005 | t0003 | g0141 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01261 | hp2 | a0003 | c0006 | t0001 | g0006 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0150 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0037 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0040 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01516 | hp1 | a0001 | c0005 | t0003 | g0250 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0015 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01517 | hp2 | a0001 | c0005 | t0003 | g0251 | EUR | IBS | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0239 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01884 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01943 | hp2 | a0001 | c0007 | t0001 | g0199 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0194 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0287 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02015 | hp1 | a0001 | c0007 | t0001 | g0158 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02055 | hp2 | a0001 | c0005 | t0003 | g0088 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0162 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02074 | hp2 | a0001 | c0007 | t0001 | g0202 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02145 | hp2 | a0001 | c0005 | t0003 | g0046 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | CDX | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02257 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02258 | hp2 | a0001 | c0005 | t0003 | g0021 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0018 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02280 | hp2 | a0001 | c0005 | t0003 | g0072 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0222 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02451 | hp2 | a0001 | c0008 | t0003 | g0207 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02572 | hp1 | a0003 | c0006 | t0001 | g0295 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02572 | hp2 | a0001 | c0005 | t0003 | g0047 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02615 | hp2 | a0001 | c0005 | t0003 | g0087 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02622 | hp1 | a0001 | c0005 | t0003 | g0238 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0050 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02630 | hp2 | a0003 | c0013 | t0003 | g0264 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0240 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02698 | hp1 | a0001 | c0004 | t0002 | g0189 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02738 | hp1 | a0001 | c0004 | t0002 | g0193 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02809 | hp1 | a0001 | c0010 | t0001 | g0056 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02818 | hp1 | a0004 | c0011 | t0001 | g0023 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02886 | hp1 | a0001 | c0005 | t0003 | g0237 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02896 | hp1 | a0001 | c0005 | t0003 | g0235 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02896 | hp2 | a0003 | c0006 | t0001 | g0006 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02897 | hp1 | a0001 | c0005 | t0003 | g0234 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02970 | hp1 | a0001 | c0005 | t0003 | g0260 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02970 | hp2 | a0003 | c0006 | t0001 | g0296 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02976 | hp1 | a0003 | c0006 | t0001 | g0262 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02976 | hp2 | a0003 | c0006 | t0002 | g0254 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03041 | hp1 | a0001 | c0009 | t0001 | g0248 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03098 | hp2 | a0001 | c0010 | t0001 | g0055 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03130 | hp1 | a0001 | c0004 | t0002 | g0243 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03130 | hp2 | a0001 | c0008 | t0003 | g0211 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0027 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03195 | hp1 | a0001 | c0005 | t0003 | g0242 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03195 | hp2 | a0003 | c0006 | t0001 | g0006 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03486 | hp1 | a0001 | c0005 | t0003 | g0085 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03486 | hp2 | a0001 | c0005 | t0003 | g0042 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03516 | hp1 | a0001 | c0008 | t0003 | g0208 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03540 | hp1 | a0001 | c0005 | t0003 | g0024 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03579 | hp1 | a0001 | c0005 | t0003 | g0084 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03688 | hp2 | a0001 | c0007 | t0006 | g0170 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03704 | hp1 | a0001 | c0004 | t0002 | g0267 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03704 | hp2 | a0001 | c0004 | t0002 | g0232 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0005 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0180 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0017 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03834 | hp2 | a0001 | c0004 | t0002 | g0212 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0246 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04184 | hp2 | a0001 | c0005 | t0003 | g0041 | SAS | BEB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04199 | hp2 | a0001 | c0004 | t0002 | g0197 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18522 | hp1 | a0005 | c0014 | t0001 | g0223 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18522 | hp2 | a0001 | c0005 | t0003 | g0021 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18950 | hp1 | a0001 | c0004 | t0002 | g0096 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0282 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18961 | hp2 | a0001 | c0004 | t0002 | g0063 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18970 | hp2 | a0001 | c0007 | t0001 | g0168 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18973 | hp2 | a0001 | c0004 | t0002 | g0101 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18978 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18978 | hp2 | a0001 | c0007 | t0001 | g0078 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0291 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0065 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0290 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19009 | hp2 | a0001 | c0007 | t0001 | g0154 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0252 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19043 | hp2 | a0001 | c0012 | t0001 | g0049 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0292 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19084 | hp2 | a0001 | c0007 | t0001 | g0201 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA19240 | hp2 | a0001 | c0005 | t0003 | g0086 | AFR | YRI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0241 | AFR | ASW | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ASW | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20805 | hp1 | a0001 | c0004 | t0002 | g0227 | EUR | TSI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0017 | SAS | GIH | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02109 | hp2 | a0001 | c0005 | t0003 | g0044 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG02559 | hp2 | a0001 | c0005 | t0003 | g0048 | AFR | ACB | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| HG06807 | hp2 | a0001 | c0009 | t0001 | g0255 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20300 | hp1 | a0003 | c0006 | t0001 | g0263 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | USA | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA21309 | hp1 | a0001 | c0004 | t0002 | g0161 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| NA21309 | hp2 | a0001 | c0004 | t0002 | g0068 | AFR | LWK | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0039 | REF | REF | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0259 | REF | REF | NOSTRIN_chr2_168797637_168870514 | NOSTRIN | chr2 | 168797637 | 168870514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168834321 | G | A | 2 | a0003 a0005 |
10 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.500G>A | p.Arg167Gln | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/16 | 510/2075 | 500/1521 | 167/506 | chr2 | 168834321 | |||
| chr2:168860868 | C | T | 2 | a0004 a0005 |
2 | HG02818.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1253C>T | p.Ala418Val | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/16 | 1263/2075 | 1253/1521 | 418/506 | chr2 | 168860868 | |||
| chr2:168864867 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
missense_variant | MODERATE | c.1418G>A | p.Gly473Glu | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 1428/2075 | 1418/1521 | 473/506 | chr2 | 168864867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168824641 | C | T | 4 | a0001c0002 a0001c0007 a0001c0008 others(1): Show |
62 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(59): Show |
synonymous_variant | LOW | c.121C>T | p.Leu41Leu | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/16 | 131/2075 | 121/1521 | 41/506 | chr2 | 168824641 | |||
| chr2:168834238 | A | G | 4 | a0001c0009 a0003c0006 a0003c0013 others(1): Show |
12 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
synonymous_variant | LOW | c.417A>G | p.Lys139Lys | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/16 | 427/2075 | 417/1521 | 139/506 | chr2 | 168834238 | |||
| chr2:168851317 | C | T | 2 | a0001c0010 a0001c0012 |
3 | HG02809.hp1 HG03098.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.768C>T | p.Asp256Asp | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/16 | 778/2075 | 768/1521 | 256/506 | chr2 | 168851317 | |||
| chr2:168859604 | T | C | 3 | a0001c0005 a0001c0008 a0003c0013 |
33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
synonymous_variant | LOW | c.1146T>C | p.Pro382Pro | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/16 | 1156/2075 | 1146/1521 | 382/506 | chr2 | 168859604 | |||
| chr2:168864871 | A | G | 2 | a0001c0002 a0001c0004 |
80 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(77): Show |
synonymous_variant | LOW | c.1422A>G | p.Gly474Gly | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 1432/2075 | 1422/1521 | 474/506 | chr2 | 168864871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168864986 | A | G | 1 | a0001c0007t0006 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*16A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 16 | chr2 | 168864986 | ||||||
| chr2:168865054 | T | C | 1 | a0001c0001t0005 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 84 | chr2 | 168865054 | ||||||
| chr2:168865130 | A | G | 3 | a0001c0005t0003 a0001c0008t0003 a0003c0013t0003 |
33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 160 | chr2 | 168865130 | ||||||
| chr2:168865390 | G | C | 1 | a0001c0001t0004 | 2 | HG02145.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 420 | chr2 | 168865390 | ||||||
| chr2:168865434 | A | T | 4 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(1): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 16/16 | 464 | chr2 | 168865434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:168802741 | G | T | 2 | a0003c0006t0001g0295 a0003c0006t0001g0296 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.27+68G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168802741 | |||||||
| chr2:168803071 | A | G | 26 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(23): Show |
27 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.27+398A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803071 | |||||||
| chr2:168803110 | A | C | 4 | a0001c0001t0002g0266 a0001c0001t0002g0269 a0001c0004t0002g0267 others(1): Show |
4 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+437A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803110 | |||||||
| chr2:168803126 | C | A | 28 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(25): Show |
29 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.27+453C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803126 | |||||||
| chr2:168803191 | T | C | 2 | a0001c0001t0002g0025 a0001c0005t0003g0007 |
3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27+518T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803191 | |||||||
| chr2:168803739 | G | A | 2 | a0001c0001t0002g0025 a0001c0005t0003g0007 |
3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.27+1066G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803739 | |||||||
| chr2:168803747 | T | A | 1 | a0002c0003t0001g0026 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.27+1074T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803747 | |||||||
| chr2:168803776 | T | G | 3 | a0001c0005t0003g0024 a0002c0003t0001g0027 a0004c0011t0001g0023 |
3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+1103T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803776 | |||||||
| chr2:168803847 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.27+1174T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803847 | |||||||
| chr2:168803912 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27+1239T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168803912 | |||||||
| chr2:168804022 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.27+1349A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804022 | |||||||
| chr2:168804177 | G | T | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+1504G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804177 | |||||||
| chr2:168804260 | C | T | 4 | a0001c0001t0001g0261 a0003c0006t0001g0262 a0003c0006t0001g0295 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+1587C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804260 | |||||||
| chr2:168804475 | G | A | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.27+1802G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804475 | |||||||
| chr2:168804750 | A | G | 29 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(26): Show |
30 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+2077A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804750 | |||||||
| chr2:168804922 | T | C | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2249T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804922 | |||||||
| chr2:168804951 | C | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(291): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.27+2278C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804951 | |||||||
| chr2:168804966 | G | T | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.27+2293G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168804966 | |||||||
| chr2:168805159 | C | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+2486C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805159 | |||||||
| chr2:168805514 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(261): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.27+2841A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805514 | |||||||
| chr2:168805687 | A | G | 3 | a0001c0005t0003g0024 a0002c0003t0001g0027 a0004c0011t0001g0023 |
3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+3014A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805687 | |||||||
| chr2:168805789 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.27+3116A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805789 | |||||||
| chr2:168805815 | C | T | 1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.27+3142C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168805815 | |||||||
| chr2:168806138 | C | T | 2 | a0001c0005t0003g0250 a0001c0005t0003g0251 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.27+3465C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806138 | |||||||
| chr2:168806183 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+3510G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806183 | |||||||
| chr2:168806226 | G | A | 4 | a0001c0001t0001g0066 a0001c0004t0002g0063 a0001c0004t0002g0065 others(1): Show |
4 | NA18954.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3553G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806226 | |||||||
| chr2:168806508 | G | A | 2 | a0001c0001t0001g0067 a0001c0004t0002g0068 |
2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.27+3835G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806508 | |||||||
| chr2:168806530 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.27+3857C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806530 | |||||||
| chr2:168806572 | GA | G | 22 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0002g0031 others(19): Show |
25 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.27+3901delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 168806572 | ||||||
| chr2:168806682 | A | G | 1 | a0001c0009t0001g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.27+4009A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806682 | |||||||
| chr2:168806787 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+4114T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806787 | |||||||
| chr2:168806899 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.27+4226C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806899 | |||||||
| chr2:168806909 | C | T | 2 | a0001c0005t0003g0024 a0004c0011t0001g0023 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.27+4236C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168806909 | |||||||
| chr2:168807283 | G | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0074 others(5): Show |
8 | HG01496.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-4284G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807283 | |||||||
| chr2:168807517 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.28-4050G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807517 | |||||||
| chr2:168807613 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.28-3954T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807613 | |||||||
| chr2:168807717 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(176): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.28-3850G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807717 | |||||||
| chr2:168807733 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-3834C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807733 | |||||||
| chr2:168807742 | G | A | 3 | a0001c0005t0003g0024 a0002c0003t0001g0027 a0004c0011t0001g0023 |
3 | HG02818.hp1 HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-3825G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807742 | |||||||
| chr2:168807757 | C | T | 1 | a0001c0002t0002g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.28-3810C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807757 | |||||||
| chr2:168807948 | A | C | 14 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(11): Show |
16 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-3619A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168807948 | |||||||
| chr2:168808019 | A | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-3548A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808019 | |||||||
| chr2:168808020 | A | G | 26 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(23): Show |
27 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-3547A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808020 | |||||||
| chr2:168808449 | C | G | 1 | a0002c0003t0001g0219 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.28-3118C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808449 | |||||||
| chr2:168808611 | A | G | 37 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0226 others(34): Show |
38 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.28-2956A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808611 | |||||||
| chr2:168808668 | A | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2899A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808668 | |||||||
| chr2:168808772 | A | G | 1 | a0001c0001t0002g0245 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.28-2795A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808772 | |||||||
| chr2:168808797 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28-2770T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808797 | |||||||
| chr2:168808810 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.28-2757A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808810 | |||||||
| chr2:168808853 | A | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2714A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168808853 | |||||||
| chr2:168809527 | A | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-2040A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809527 | |||||||
| chr2:168809591 | C | A | 2 | a0001c0005t0003g0024 a0004c0011t0001g0023 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-1976C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809591 | |||||||
| chr2:168809620 | A | C | 1 | a0003c0006t0001g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.28-1947A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168809620 | |||||||
| chr2:168810039 | T | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0261 a0003c0006t0001g0262 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-1528T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810039 | |||||||
| chr2:168810235 | A | G | 31 | a0001c0001t0001g0265 a0001c0001t0001g0271 a0001c0001t0001g0272 others(28): Show |
32 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.28-1332A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810235 | |||||||
| chr2:168810590 | T | G | 1 | a0002c0003t0001g0270 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.28-977T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810590 | |||||||
| chr2:168810918 | A | C | 2 | a0001c0005t0003g0024 a0004c0011t0001g0023 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.28-649A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810918 | |||||||
| chr2:168810944 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02738.hp2 HG03490.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.28-623C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810944 | |||||||
| chr2:168810945 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG00423.hp1 HG02027.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.28-622G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810945 | |||||||
| chr2:168810985 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(122): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.28-582T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168810985 | |||||||
| chr2:168811182 | T | G | 3 | a0001c0002t0002g0157 a0001c0002t0002g0159 a0001c0007t0001g0158 |
3 | HG00438.hp2 HG02015.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.28-385T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811182 | |||||||
| chr2:168811284 | A | T | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-283A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811284 | |||||||
| chr2:168811418 | T | C | 1 | a0001c0007t0001g0078 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.28-149T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 1/15 | chr2 | 168811418 | |||||||
| chr2:168812010 | G | A | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+358G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812010 | |||||||
| chr2:168812118 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0002g0052 a0001c0001t0002g0053 others(2): Show |
6 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+466G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812118 | |||||||
| chr2:168812160 | T | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0261 a0001c0001t0001g0265 others(3): Show |
6 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+508T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812160 | |||||||
| chr2:168812451 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.113+799G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812451 | |||||||
| chr2:168812521 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(200): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.113+869T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812521 | |||||||
| chr2:168812532 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.113+880C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812532 | |||||||
| chr2:168812799 | G | T | 1 | a0001c0002t0002g0214 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.113+1147G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812799 | |||||||
| chr2:168812952 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(106): Show |
119 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+1300G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168812952 | |||||||
| chr2:168813014 | AC | A | 71 | a0001c0001t0001g0165 a0001c0001t0001g0187 a0001c0001t0001g0188 others(68): Show |
83 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.113+1363delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813014 | |||||||
| chr2:168813067 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.113+1415A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813067 | |||||||
| chr2:168813198 | C | T | 14 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(11): Show |
16 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.113+1546C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813198 | |||||||
| chr2:168813269 | G | A | 26 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0226 others(23): Show |
27 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.113+1617G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813269 | |||||||
| chr2:168813451 | T | C | 75 | a0001c0001t0001g0165 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
87 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.113+1799T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813451 | |||||||
| chr2:168813552 | G | A | 1 | a0001c0002t0002g0162 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.113+1900G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813552 | |||||||
| chr2:168813725 | G | C | 1 | a0001c0005t0003g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.113+2073G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168813725 | |||||||
| chr2:168813776 | TACAAAGA others(9): Show |
T | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.113+2126_113+2141d others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168813776 | ||||||
| chr2:168814022 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.113+2370T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814022 | |||||||
| chr2:168814051 | A | C | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
8 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+2399A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814051 | |||||||
| chr2:168814219 | C | T | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+2567C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814219 | |||||||
| chr2:168814302 | A | T | 2 | a0001c0005t0003g0024 a0004c0011t0001g0023 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+2650A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814302 | |||||||
| chr2:168814651 | C | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0261 a0003c0006t0001g0262 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+2999C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814651 | |||||||
| chr2:168814654 | T | C | 1 | a0001c0005t0003g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+3002T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814654 | |||||||
| chr2:168814693 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(152): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.113+3041A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168814693 | |||||||
| chr2:168814697 | AAGG | A | 4 | a0001c0001t0001g0067 a0001c0004t0002g0068 a0001c0004t0002g0243 others(1): Show |
4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+3050_113+3052d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168814697 | ||||||
| chr2:168815225 | A | G | 29 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(26): Show |
30 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+3573A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815225 | |||||||
| chr2:168815304 | G | C | 2 | a0001c0005t0003g0024 a0004c0011t0001g0023 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+3652G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815304 | |||||||
| chr2:168815327 | T | G | 1 | a0001c0004t0002g0163 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.113+3675T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815327 | |||||||
| chr2:168815437 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.113+3785T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815437 | |||||||
| chr2:168815443 | C | G | 1 | a0001c0004t0002g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+3791C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815443 | |||||||
| chr2:168815829 | T | C | 4 | a0001c0001t0001g0067 a0001c0004t0002g0068 a0001c0004t0002g0243 others(1): Show |
4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+4177T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168815829 | |||||||
| chr2:168816037 | G | T | 1 | a0001c0001t0001g0010 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.113+4385G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816037 | |||||||
| chr2:168816115 | G | A | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+4463G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816115 | |||||||
| chr2:168816123 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(291): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.113+4471A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816123 | |||||||
| chr2:168816291 | A | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.113+4639A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816291 | |||||||
| chr2:168816369 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0054 a0001c0001t0001g0067 others(41): Show |
48 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.113+4717C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816369 | |||||||
| chr2:168816413 | C | T | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.113+4761C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816413 | |||||||
| chr2:168816515 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.113+4863G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816515 | |||||||
| chr2:168816899 | G | A | 40 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(37): Show |
43 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+5247G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168816899 | |||||||
| chr2:168817045 | A | G | 2 | a0001c0005t0003g0250 a0001c0005t0003g0251 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.113+5393A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817045 | |||||||
| chr2:168817066 | G | A | 40 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(37): Show |
43 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+5414G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817066 | |||||||
| chr2:168817104 | C | A | 40 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(37): Show |
43 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+5452C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817104 | |||||||
| chr2:168817108 | A | G | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+5456A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817108 | |||||||
| chr2:168817289 | CAG | C | 6 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0004t0002g0222 others(3): Show |
6 | HG02451.hp1 HG02451.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+5640_113+5641d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168817289 | ||||||
| chr2:168817301 | G | A | 3 | a0001c0001t0001g0054 a0001c0010t0001g0055 a0001c0010t0001g0056 |
3 | HG02809.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.113+5649G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817301 | |||||||
| chr2:168817357 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(112): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.113+5705T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817357 | |||||||
| chr2:168817379 | G | A | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+5727G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817379 | |||||||
| chr2:168817383 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5731A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817383 | |||||||
| chr2:168817469 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5817A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817469 | |||||||
| chr2:168817498 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5846A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817498 | |||||||
| chr2:168817557 | AC | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(161): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.113+5906delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817557 | |||||||
| chr2:168817589 | C | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0269 a0001c0004t0002g0218 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+5937C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817589 | |||||||
| chr2:168817632 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(162): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.113+5980T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817632 | |||||||
| chr2:168817645 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113+5993T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817645 | |||||||
| chr2:168817665 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.113+6013C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817665 | |||||||
| chr2:168817669 | C | T | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.113+6017C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817669 | |||||||
| chr2:168817672 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(167): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.113+6020T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817672 | |||||||
| chr2:168817869 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(165): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.113+6217A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168817869 | |||||||
| chr2:168818145 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(265): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.114-6489T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818145 | |||||||
| chr2:168818153 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(265): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.114-6481A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818153 | |||||||
| chr2:168818180 | T | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0271 a0001c0001t0001g0272 others(15): Show |
20 | HG00558.hp2 HG00673.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-6454T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818180 | |||||||
| chr2:168818206 | T | G | 6 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(3): Show |
8 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-6428T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818206 | |||||||
| chr2:168818254 | C | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(203): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.114-6380C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818254 | |||||||
| chr2:168818296 | G | C | 70 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(67): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.114-6338G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818296 | |||||||
| chr2:168818547 | C | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
9 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.114-6087C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818547 | |||||||
| chr2:168818598 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0261 a0001c0001t0002g0052 others(1): Show |
5 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-6036G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818598 | |||||||
| chr2:168818600 | G | A | 1 | a0002c0003t0001g0026 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.114-6034G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818600 | |||||||
| chr2:168818615 | T | C | 1 | a0001c0009t0001g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.114-6019T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168818615 | |||||||
| chr2:168818841 | A | AT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(210): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.114-5786dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168818841 | ||||||
| chr2:168818952 | AAT | A | 20 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(17): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-5675_114-5674d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168818952 | ||||||
| chr2:168819046 | G | GA | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(283): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.114-5581dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168819046 | ||||||
| chr2:168819056 | C | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(209): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.114-5578C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819056 | |||||||
| chr2:168819083 | G | A | 1 | a0002c0003t0001g0015 | 2 | HG01516.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.114-5551G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819083 | |||||||
| chr2:168819109 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
15 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.114-5525T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819109 | |||||||
| chr2:168819251 | G | A | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114-5383G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819251 | |||||||
| chr2:168819347 | C | T | 2 | a0001c0007t0001g0201 a0001c0007t0001g0202 |
2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.114-5287C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819347 | |||||||
| chr2:168819377 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.114-5257A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819377 | |||||||
| chr2:168819454 | C | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.114-5180C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819454 | |||||||
| chr2:168819535 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(206): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.114-5099G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819535 | |||||||
| chr2:168819575 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.114-5059T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819575 | |||||||
| chr2:168819843 | G | T | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-4791G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819843 | |||||||
| chr2:168819900 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114-4734A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819900 | |||||||
| chr2:168819957 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.114-4677C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819957 | |||||||
| chr2:168819965 | C | T | 3 | a0001c0001t0001g0054 a0001c0010t0001g0055 a0001c0010t0001g0056 |
3 | HG02809.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.114-4669C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168819965 | |||||||
| chr2:168820011 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(291): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.114-4623T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820011 | |||||||
| chr2:168820071 | G | T | 2 | a0001c0005t0003g0250 a0001c0005t0003g0251 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.114-4563G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820071 | |||||||
| chr2:168820241 | C | T | 77 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0165 others(74): Show |
89 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.114-4393C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820241 | |||||||
| chr2:168820258 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0203 a0001c0001t0002g0205 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-4376G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820258 | |||||||
| chr2:168820276 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.114-4358T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820276 | |||||||
| chr2:168820374 | G | A | 12 | a0001c0001t0002g0031 a0002c0003t0001g0008 a0002c0003t0001g0009 others(9): Show |
14 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.114-4260G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820374 | |||||||
| chr2:168820718 | C | CA | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(163): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.114-3903dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | ||||||
| chr2:168820718 | C | CAA | 89 | a0001c0001t0001g0082 a0001c0001t0001g0089 a0001c0001t0001g0090 others(86): Show |
103 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.114-3904_114-3903d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | ||||||
| chr2:168820718 | C | CAAA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0203 others(9): Show |
13 | HG01891.hp1 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.114-3905_114-3903d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820718 | ||||||
| chr2:168820734 | C | T | 3 | a0001c0009t0001g0248 a0002c0003t0001g0240 a0002c0003t0001g0241 |
3 | HG02647.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-3900C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820734 | |||||||
| chr2:168820760 | A | AC | 4 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0004t0002g0279 others(1): Show |
4 | HG00673.hp2 HG00733.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-3870dupC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168820760 | ||||||
| chr2:168820778 | C | A | 1 | a0002c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.114-3856C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820778 | |||||||
| chr2:168820788 | C | T | 1 | a0002c0003t0001g0026 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.114-3846C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820788 | |||||||
| chr2:168820835 | G | A | 1 | a0001c0005t0003g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114-3799G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820835 | |||||||
| chr2:168820918 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114-3716T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820918 | |||||||
| chr2:168820943 | C | T | 1 | a0002c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.114-3691C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820943 | |||||||
| chr2:168820948 | A | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114-3686A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168820948 | |||||||
| chr2:168821010 | G | T | 2 | a0001c0004t0002g0243 a0001c0005t0003g0242 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.114-3624G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821010 | |||||||
| chr2:168821687 | C | T | 73 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(70): Show |
85 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.114-2947C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821687 | |||||||
| chr2:168821688 | G | A | 20 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(17): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-2946G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821688 | |||||||
| chr2:168821702 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.114-2932G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821702 | |||||||
| chr2:168821863 | C | T | 4 | a0001c0001t0002g0057 a0001c0009t0001g0248 a0002c0003t0001g0240 others(1): Show |
4 | HG02647.hp1 HG03041.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2771C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821863 | |||||||
| chr2:168821982 | T | C | 1 | a0002c0003t0001g0240 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114-2652T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168821982 | |||||||
| chr2:168822051 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0142 a0001c0001t0001g0143 others(1): Show |
4 | NA18948.hp2 NA18992.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2583C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822051 | |||||||
| chr2:168822171 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(211): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.114-2463T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822171 | |||||||
| chr2:168822182 | T | C | 4 | a0001c0001t0001g0067 a0001c0004t0002g0068 a0001c0004t0002g0243 others(1): Show |
4 | HG00733.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-2452T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822182 | |||||||
| chr2:168822195 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114-2439T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822195 | |||||||
| chr2:168822347 | GA | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(204): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.114-2277delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 168822347 | ||||||
| chr2:168822418 | A | G | 1 | a0001c0002t0002g0198 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.114-2216A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822418 | |||||||
| chr2:168822491 | A | G | 1 | a0002c0003t0001g0083 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.114-2143A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822491 | |||||||
| chr2:168822540 | A | G | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.114-2094A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822540 | |||||||
| chr2:168822675 | C | T | 1 | a0001c0004t0002g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.114-1959C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822675 | |||||||
| chr2:168822971 | C | G | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG06807.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114-1663C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822971 | |||||||
| chr2:168822972 | A | C | 1 | a0001c0001t0002g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-1662A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168822972 | |||||||
| chr2:168823085 | T | G | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0089 others(9): Show |
12 | HG01943.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-1549T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823085 | |||||||
| chr2:168823174 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(283): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.114-1460A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823174 | |||||||
| chr2:168823217 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-1417T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823217 | |||||||
| chr2:168823238 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114-1396G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823238 | |||||||
| chr2:168823251 | T | CGTGATCC others(127): Show |
1 | a0001c0002t0002g0293 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.114-1384_114-1383i others(136): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823251 | |||||||
| chr2:168823279 | A | G | 1 | a0001c0004t0002g0243 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-1355A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823279 | |||||||
| chr2:168823307 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02056.hp1 HG02071.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.114-1327C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823307 | |||||||
| chr2:168823347 | A | C | 1 | a0001c0002t0002g0288 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.114-1287A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823347 | |||||||
| chr2:168823569 | G | A | 15 | a0001c0001t0002g0031 a0001c0005t0003g0024 a0002c0003t0001g0008 others(12): Show |
17 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.114-1065G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823569 | |||||||
| chr2:168823577 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0261 |
3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.114-1057A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823577 | |||||||
| chr2:168823612 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(212): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.114-1022C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823612 | |||||||
| chr2:168823847 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-787C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823847 | |||||||
| chr2:168823869 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-765G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168823869 | |||||||
| chr2:168824173 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.114-461T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824173 | |||||||
| chr2:168824267 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(220): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.114-367A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824267 | |||||||
| chr2:168824456 | G | A | 1 | a0005c0014t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.114-178G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824456 | |||||||
| chr2:168824610 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.114-24A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 2/15 | chr2 | 168824610 | |||||||
| chr2:168824725 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA20129.hp2 | splice_region_variant&intron_variant | LOW | c.197+8T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824725 | |||||||
| chr2:168824760 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0261 a0001c0001t0002g0052 others(1): Show |
5 | HG01891.hp1 HG02615.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+43T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824760 | |||||||
| chr2:168824768 | T | TTTTGTTT others(1): Show |
54 | a0001c0001t0001g0010 a0001c0001t0001g0187 a0001c0001t0001g0188 others(51): Show |
64 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.197+67_197+74dupGT others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | ||||||
| chr2:168824768 | T | TTTTGTTT others(5): Show |
145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(142): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.197+63_197+74dupGT others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | ||||||
| chr2:168824768 | T | TTTTGTTT others(9): Show |
14 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0097 others(11): Show |
14 | HG01993.hp2 HG02056.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.197+59_197+74dupGT others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | ||||||
| chr2:168824768 | T | TTTTGTTT others(13): Show |
1 | a0001c0001t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.197+55_197+74dupGT others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168824768 | ||||||
| chr2:168824833 | G | T | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+116G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824833 | |||||||
| chr2:168824888 | C | T | 2 | a0001c0004t0002g0051 a0001c0004t0002g0222 |
2 | HG01074.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.197+171C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824888 | |||||||
| chr2:168824915 | G | A | 2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.197+198G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824915 | |||||||
| chr2:168824916 | G | C | 2 | a0001c0002t0002g0166 a0001c0002t0002g0167 |
2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.197+199G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168824916 | |||||||
| chr2:168825019 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(174): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.197+302A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825019 | |||||||
| chr2:168825239 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(166): Show |
186 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.197+522G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825239 | |||||||
| chr2:168825397 | G | A | 2 | a0001c0001t0002g0025 a0001c0005t0003g0007 |
3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.197+680G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825397 | |||||||
| chr2:168825668 | TA | T | 5 | a0001c0005t0003g0084 a0001c0005t0003g0085 a0001c0005t0003g0086 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+952delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825668 | |||||||
| chr2:168825745 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.197+1028T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825745 | |||||||
| chr2:168825867 | A | G | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+1150A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168825867 | |||||||
| chr2:168826200 | C | T | 30 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(27): Show |
35 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.197+1483C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826200 | |||||||
| chr2:168826220 | G | GAGAGGTA others(1): Show |
24 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(21): Show |
27 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.197+1505_197+1506i others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826220 | ||||||
| chr2:168826220 | G | GAGGGGTG others(1): Show |
257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(254): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.197+1512_197+1519d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826220 | ||||||
| chr2:168826221 | A | AGAGGTAT | 4 | a0002c0003t0001g0015 a0002c0003t0001g0019 a0002c0003t0001g0246 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+1505_197+1506i others(9): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 168826221 | ||||||
| chr2:168826354 | A | T | 2 | a0001c0002t0002g0159 a0001c0007t0001g0158 |
2 | HG00438.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.197+1637A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826354 | |||||||
| chr2:168826446 | T | C | 77 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(74): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.198-1712T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826446 | |||||||
| chr2:168826456 | T | C | 105 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(102): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.198-1702T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826456 | |||||||
| chr2:168826479 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.198-1679T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826479 | |||||||
| chr2:168826527 | C | T | 1 | a0001c0004t0002g0065 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.198-1631C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826527 | |||||||
| chr2:168826551 | G | A | 28 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(25): Show |
33 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.198-1607G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826551 | |||||||
| chr2:168826698 | G | A | 2 | a0001c0001t0002g0025 a0001c0005t0003g0007 |
3 | HG01884.hp2 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.198-1460G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826698 | |||||||
| chr2:168826915 | C | T | 8 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0097 others(5): Show |
8 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-1243C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168826915 | |||||||
| chr2:168827041 | G | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.198-1117G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827041 | |||||||
| chr2:168827141 | C | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-1017C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827141 | |||||||
| chr2:168827160 | C | G | 1 | a0005c0014t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-998C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827160 | |||||||
| chr2:168827241 | A | G | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.198-917A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827241 | |||||||
| chr2:168827417 | G | A | 40 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0200 others(37): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.198-741G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827417 | |||||||
| chr2:168827471 | A | G | 1 | a0005c0014t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-687A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827471 | |||||||
| chr2:168827598 | C | T | 8 | a0001c0004t0002g0222 a0001c0005t0003g0021 a0001c0005t0003g0234 others(5): Show |
9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.198-560C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827598 | |||||||
| chr2:168827606 | C | T | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-552C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827606 | |||||||
| chr2:168827632 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18997.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.198-526G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827632 | |||||||
| chr2:168827713 | G | A | 1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198-445G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827713 | |||||||
| chr2:168827947 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(281): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.198-211A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827947 | |||||||
| chr2:168827952 | G | C | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198-206G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827952 | |||||||
| chr2:168827960 | G | A | 1 | a0001c0004t0002g0227 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.198-198G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168827960 | |||||||
| chr2:168828123 | A | G | 18 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(15): Show |
19 | HG00423.hp1 HG00673.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-35A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 3/15 | chr2 | 168828123 | |||||||
| chr2:168828240 | C | G | 8 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0097 others(5): Show |
8 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.260+20C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 4/15 | chr2 | 168828240 | |||||||
| chr2:168828761 | A | G | 1 | a0002c0003t0001g0150 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.342+260A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828761 | |||||||
| chr2:168828762 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(203): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.342+261A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828762 | |||||||
| chr2:168828776 | A | G | 1 | a0001c0002t0002g0288 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.342+275A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828776 | |||||||
| chr2:168828819 | T | C | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.342+318T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168828819 | |||||||
| chr2:168829246 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(126): Show |
140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.342+745A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829246 | |||||||
| chr2:168829343 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.342+842G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829343 | |||||||
| chr2:168829477 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.342+976C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829477 | |||||||
| chr2:168829518 | G | A | 3 | a0001c0001t0002g0057 a0002c0003t0001g0240 a0002c0003t0001g0241 |
3 | HG02647.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.342+1017G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829518 | |||||||
| chr2:168829520 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(267): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.342+1019T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829520 | |||||||
| chr2:168829619 | C | T | 7 | a0001c0005t0003g0021 a0001c0005t0003g0234 a0001c0005t0003g0235 others(4): Show |
8 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.342+1118C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829619 | |||||||
| chr2:168829789 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.342+1288A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168829789 | |||||||
| chr2:168830049 | C | T | 88 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0002g0266 others(85): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.343-1423C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830049 | |||||||
| chr2:168830148 | G | A | 2 | a0003c0006t0001g0295 a0003c0006t0001g0296 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.343-1324G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830148 | |||||||
| chr2:168830293 | T | C | 1 | a0001c0007t0006g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.343-1179T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830293 | |||||||
| chr2:168830547 | G | T | 1 | a0001c0002t0002g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.343-925G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830547 | |||||||
| chr2:168830637 | A | G | 1 | a0001c0004t0002g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.343-835A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830637 | |||||||
| chr2:168830701 | T | C | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-771T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830701 | |||||||
| chr2:168830831 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(133): Show |
149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.343-641C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830831 | |||||||
| chr2:168830849 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(79): Show |
90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.343-623G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830849 | |||||||
| chr2:168830909 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.343-563A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168830909 | |||||||
| chr2:168831170 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(270): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.343-302A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168831170 | |||||||
| chr2:168831247 | A | C | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.343-225A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 5/15 | chr2 | 168831247 | |||||||
| chr2:168831558 | G | T | 1 | a0001c0004t0002g0065 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.405+24G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831558 | |||||||
| chr2:168831645 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+111T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831645 | |||||||
| chr2:168831869 | A | G | 2 | a0003c0006t0002g0254 a0005c0014t0001g0223 |
2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.405+335A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168831869 | |||||||
| chr2:168832189 | AATTTAGT others(7): Show |
A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0005t0003g0041 others(8): Show |
11 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.405+658_405+671del others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 168832189 | ||||||
| chr2:168832209 | G | A | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.405+675G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832209 | |||||||
| chr2:168832237 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(190): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.405+703G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832237 | |||||||
| chr2:168832370 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.405+836G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832370 | |||||||
| chr2:168832532 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.405+998G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832532 | |||||||
| chr2:168832760 | G | T | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+1226G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832760 | |||||||
| chr2:168832822 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.405+1288A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832822 | |||||||
| chr2:168832837 | A | G | 68 | a0001c0001t0001g0188 a0001c0001t0001g0200 a0001c0001t0002g0266 others(65): Show |
78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.405+1303A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168832837 | |||||||
| chr2:168833022 | T | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(30): Show |
34 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.406-1205T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833022 | |||||||
| chr2:168833131 | G | A | 10 | a0001c0009t0001g0248 a0001c0009t0001g0255 a0003c0006t0001g0006 others(7): Show |
12 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.406-1096G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833131 | |||||||
| chr2:168833166 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(160): Show |
175 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.406-1061C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833166 | |||||||
| chr2:168833220 | G | A | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.406-1007G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833220 | |||||||
| chr2:168833261 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(190): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.406-966G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833261 | |||||||
| chr2:168833267 | C | G | 3 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 |
3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.406-960C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833267 | |||||||
| chr2:168833396 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.406-831C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833396 | |||||||
| chr2:168833425 | C | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-802C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833425 | |||||||
| chr2:168833532 | T | C | 1 | a0002c0003t0001g0027 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.406-695T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833532 | |||||||
| chr2:168833579 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(271): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.406-648C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833579 | |||||||
| chr2:168833705 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-522G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833705 | |||||||
| chr2:168833748 | G | T | 2 | a0003c0006t0001g0295 a0003c0006t0001g0296 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.406-479G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833748 | |||||||
| chr2:168833816 | CA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(190): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.406-408delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 168833816 | ||||||
| chr2:168833899 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.406-328T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833899 | |||||||
| chr2:168833912 | A | G | 1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.406-315A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168833912 | |||||||
| chr2:168834001 | G | A | 1 | a0002c0003t0001g0032 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.406-226G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834001 | |||||||
| chr2:168834118 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.406-109A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834118 | |||||||
| chr2:168834219 | T | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(179): Show |
195 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
splice_region_variant&intron_variant | LOW | c.406-8T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 6/15 | chr2 | 168834219 | |||||||
| chr2:168834406 | G | A | 1 | a0001c0002t0002g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.504+81G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834406 | |||||||
| chr2:168834479 | C | A | 1 | a0001c0002t0002g0171 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.504+154C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834479 | |||||||
| chr2:168834490 | T | C | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+165T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834490 | |||||||
| chr2:168834490 | T | TGC | 5 | a0001c0005t0003g0024 a0002c0003t0001g0015 a0002c0003t0001g0027 others(2): Show |
6 | HG01099.hp1 HG01496.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+182_504+183dup others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834490 | ||||||
| chr2:168834493 | GCGCGCGC others(15): Show |
G | 1 | a0002c0003t0001g0291 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.504+170_504+191del others(22): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834493 | ||||||
| chr2:168834493 | GCGCGCGC others(17): Show |
G | 18 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(15): Show |
19 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.504+170_504+193del others(24): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834493 | ||||||
| chr2:168834497 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504+172G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834497 | |||||||
| chr2:168834499 | G | GCACACAC others(5): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
8 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+175_504+176ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | ||||||
| chr2:168834499 | G | GCACACAC others(7): Show |
1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.504+175_504+176ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | ||||||
| chr2:168834499 | G | GCGCACAC others(9): Show |
2 | a0003c0006t0001g0006 a0003c0013t0003g0264 |
3 | HG01261.hp2 HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.504+177_504+178ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | ||||||
| chr2:168834499 | G | GCGCGCAC others(9): Show |
1 | a0005c0014t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.504+179_504+180ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834499 | ||||||
| chr2:168834500 | C | T | 2 | a0001c0001t0001g0067 a0001c0004t0002g0068 |
2 | HG00733.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504+175C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834500 | |||||||
| chr2:168834501 | G | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(13): Show |
17 | HG01070.hp1 HG01496.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.504+176G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834501 | |||||||
| chr2:168834501 | G | GCACACAC others(3): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0138 others(2): Show |
5 | HG00438.hp1 HG01261.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | ||||||
| chr2:168834501 | G | GCACACAC others(5): Show |
41 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(38): Show |
46 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | ||||||
| chr2:168834501 | G | GCACACAC others(7): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0261 others(7): Show |
11 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.504+177_504+178ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | ||||||
| chr2:168834501 | G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0090 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.504+177_504+178ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834501 | ||||||
| chr2:168834502 | C | A | 1 | a0001c0007t0001g0078 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.504+177C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834502 | |||||||
| chr2:168834503 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(150): Show |
165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.504+178G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834503 | |||||||
| chr2:168834503 | G | GCACA | 3 | a0001c0008t0003g0207 a0001c0008t0003g0208 a0001c0008t0003g0211 |
3 | HG02451.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.504+179_504+180ins others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | ||||||
| chr2:168834503 | G | GCACACAC others(3): Show |
1 | a0003c0006t0001g0262 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+179_504+180ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | ||||||
| chr2:168834503 | G | GCACACAC others(9): Show |
1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.504+179_504+180ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834503 | ||||||
| chr2:168834505 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(160): Show |
173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.504+180G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834505 | |||||||
| chr2:168834505 | G | GCACACAC others(7): Show |
1 | a0001c0005t0003g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.504+181_504+182ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834505 | ||||||
| chr2:168834505 | G | GCAGCGCG others(12): Show |
1 | a0001c0002t0002g0177 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.504+181_504+182ins others(19): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834505 | ||||||
| chr2:168834507 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
136 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.504+182G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834507 | |||||||
| chr2:168834507 | G | GCACACAC others(3): Show |
4 | a0001c0002t0002g0004 a0001c0002t0002g0186 a0001c0002t0002g0293 others(1): Show |
4 | HG00408.hp1 HG01168.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+208_504+217dup others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCAGCGCG others(20): Show |
1 | a0001c0005t0003g0251 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.504+184_504+185ins others(27): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCACAC others(3): Show |
3 | a0001c0002t0002g0020 a0001c0002t0002g0220 a0001c0004t0002g0267 |
3 | HG00621.hp1 HG03704.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCACAC others(5): Show |
8 | a0001c0001t0001g0258 a0001c0002t0002g0004 a0001c0002t0002g0017 others(5): Show |
8 | HG01070.hp1 HG01074.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCACAC others(7): Show |
3 | a0001c0001t0001g0043 a0001c0004t0002g0218 a0001c0004t0002g0243 |
3 | HG01175.hp2 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCACAC others(9): Show |
1 | a0001c0005t0003g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(3): Show |
4 | a0001c0001t0001g0188 a0001c0002t0002g0003 a0001c0002t0002g0162 others(1): Show |
4 | HG02071.hp2 HG02602.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(5): Show |
7 | a0001c0002t0002g0004 a0001c0002t0002g0017 a0001c0002t0002g0180 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(7): Show |
11 | a0001c0002t0002g0003 a0001c0002t0002g0195 a0001c0002t0002g0214 others(8): Show |
12 | HG00323.hp1 HG02015.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(9): Show |
1 | a0001c0002t0002g0183 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(11): Show |
1 | a0001c0002t0002g0020 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCAC others(13): Show |
1 | a0001c0002t0002g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(20): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(3): Show |
1 | a0001c0004t0002g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(5): Show |
6 | a0001c0002t0002g0079 a0001c0002t0002g0164 a0001c0002t0002g0174 others(3): Show |
6 | HG00738.hp1 HG03688.hp2 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(7): Show |
8 | a0001c0002t0002g0080 a0001c0002t0002g0159 a0001c0002t0002g0167 others(5): Show |
8 | HG00438.hp2 HG01256.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(9): Show |
2 | a0001c0002t0002g0166 a0001c0002t0002g0169 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(11): Show |
1 | a0001c0002t0002g0185 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(7): Show |
2 | a0001c0001t0001g0200 a0001c0002t0002g0171 |
2 | HG00673.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.504+183_504+184ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(9): Show |
1 | a0001c0002t0002g0182 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(11): Show |
1 | a0001c0002t0002g0178 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.504+183_504+184ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(5): Show |
1 | a0001c0005t0003g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(19): Show |
1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(26): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | G | GCGCGCGC others(21): Show |
1 | a0001c0005t0003g0250 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.504+183_504+184ins others(28): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834507 | GCA | G | 9 | a0002c0003t0001g0008 a0002c0003t0001g0009 a0002c0003t0001g0026 others(6): Show |
10 | HG00099.hp1 HG01069.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.504+216_504+217del others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834507 | ||||||
| chr2:168834509 | A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0265 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | HG02615.hp1 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834509 | ||||||
| chr2:168834509 | A | G | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(39): Show |
46 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.504+184A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834509 | |||||||
| chr2:168834511 | A | ACACACAC others(5): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0278 |
2 | HG03831.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.504+195_504+196ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | ||||||
| chr2:168834511 | A | ACACACAC others(1): Show |
4 | a0001c0001t0001g0203 a0001c0001t0002g0205 a0001c0001t0004g0204 others(1): Show |
4 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | ||||||
| chr2:168834511 | A | ACACACAC others(3): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
48 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | ||||||
| chr2:168834511 | A | ACACACG | 4 | a0001c0001t0001g0054 a0001c0009t0001g0255 a0001c0010t0001g0055 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+191_504+192ins others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834511 | ||||||
| chr2:168834511 | A | G | 1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.504+186A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834511 | |||||||
| chr2:168834513 | A | ACACACGC others(1): Show |
8 | a0001c0001t0001g0112 a0001c0001t0001g0137 a0001c0001t0001g0142 others(5): Show |
8 | HG02056.hp2 HG03209.hp1 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.504+193_504+194ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834513 | ||||||
| chr2:168834517 | A | ACGCGCAC others(3): Show |
1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.504+193_504+194ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834517 | ||||||
| chr2:168834541 | A | ACACACAC others(4): Show |
1 | a0001c0004t0002g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.504+217_504+218ins others(11): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACAC others(11): Show |
1 | a0001c0001t0002g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.504+217_504+218ins others(18): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACAC others(7): Show |
2 | a0001c0001t0001g0067 a0001c0001t0002g0108 |
2 | HG00733.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.504+217_504+218ins others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACAC others(5): Show |
7 | a0001c0001t0001g0148 a0001c0001t0002g0071 a0001c0001t0002g0109 others(4): Show |
7 | HG00642.hp2 HG00735.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(12): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACAC others(3): Show |
5 | a0001c0001t0001g0231 a0001c0005t0003g0234 a0001c0005t0003g0235 others(2): Show |
5 | HG01255.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACAC others(1): Show |
10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0031 others(7): Show |
11 | HG01358.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | ACACACC | 4 | a0001c0001t0001g0233 a0001c0001t0002g0030 a0001c0001t0002g0073 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+217_504+218ins others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834541 | ||||||
| chr2:168834541 | A | C | 21 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(18): Show |
22 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.504+216A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834541 | |||||||
| chr2:168834542 | C | CACACACA others(6): Show |
1 | a0001c0002t0002g0172 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.504+217_504+218ins others(13): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834542 | |||||||
| chr2:168834600 | G | GC | 11 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0005t0003g0041 others(8): Show |
11 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+278dupC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168834600 | ||||||
| chr2:168834677 | A | G | 8 | a0001c0005t0003g0021 a0001c0005t0003g0234 a0001c0005t0003g0235 others(5): Show |
9 | HG01255.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.504+352A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834677 | |||||||
| chr2:168834762 | A | G | 9 | a0001c0001t0001g0070 a0001c0001t0001g0089 a0001c0001t0001g0095 others(6): Show |
9 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+437A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834762 | |||||||
| chr2:168834773 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.504+448A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834773 | |||||||
| chr2:168834802 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+477A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168834802 | |||||||
| chr2:168835030 | C | G | 9 | a0001c0001t0001g0070 a0001c0001t0001g0089 a0001c0001t0001g0095 others(6): Show |
9 | HG01943.hp1 HG02056.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+705C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835030 | |||||||
| chr2:168835208 | G | A | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+883G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835208 | |||||||
| chr2:168835235 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.504+910C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835235 | |||||||
| chr2:168835241 | A | AT | 18 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0058 others(15): Show |
19 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.504+925dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168835241 | ||||||
| chr2:168835265 | G | C | 1 | a0001c0001t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.504+940G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835265 | |||||||
| chr2:168835299 | G | A | 3 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 |
3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.504+974G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835299 | |||||||
| chr2:168835396 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.504+1071A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835396 | |||||||
| chr2:168835448 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+1123T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835448 | |||||||
| chr2:168835460 | C | A | 6 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0164 others(3): Show |
6 | NA18943.hp1 NA18951.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+1135C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835460 | |||||||
| chr2:168835472 | C | T | 1 | a0001c0009t0001g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.504+1147C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835472 | |||||||
| chr2:168835859 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(117): Show |
131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.504+1534G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835859 | |||||||
| chr2:168835927 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.504+1602T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168835927 | |||||||
| chr2:168836050 | A | C | 4 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0164 others(1): Show |
4 | NA18970.hp1 NA19054.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+1725A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836050 | |||||||
| chr2:168836132 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(189): Show |
207 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.504+1807C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836132 | |||||||
| chr2:168836155 | A | T | 1 | a0001c0007t0001g0202 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.504+1830A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836155 | |||||||
| chr2:168836207 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+1882A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836207 | |||||||
| chr2:168836298 | A | C | 2 | a0001c0005t0003g0250 a0001c0005t0003g0251 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.504+1973A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836298 | |||||||
| chr2:168836530 | C | A | 1 | a0001c0002t0002g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.504+2205C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836530 | |||||||
| chr2:168836538 | A | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0029 |
2 | HG02257.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.504+2213A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836538 | |||||||
| chr2:168836599 | C | G | 3 | a0001c0009t0001g0248 a0003c0006t0002g0254 a0005c0014t0001g0223 |
3 | HG02976.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.504+2274C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836599 | |||||||
| chr2:168836631 | C | G | 2 | a0001c0009t0001g0248 a0005c0014t0001g0223 |
2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.504+2306C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836631 | |||||||
| chr2:168836734 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.504+2409A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836734 | |||||||
| chr2:168836904 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(192): Show |
210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.504+2579T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836904 | |||||||
| chr2:168836980 | T | A | 54 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(51): Show |
56 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.504+2655T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168836980 | |||||||
| chr2:168837027 | A | G | 51 | a0001c0001t0001g0258 a0001c0002t0002g0003 a0001c0002t0002g0004 others(48): Show |
58 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.504+2702A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837027 | |||||||
| chr2:168837164 | C | A | 4 | a0003c0006t0001g0262 a0003c0006t0001g0263 a0003c0006t0001g0295 others(1): Show |
4 | HG02572.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+2839C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837164 | |||||||
| chr2:168837298 | A | G | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+2973A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837298 | |||||||
| chr2:168837300 | C | CT | 79 | a0001c0001t0001g0062 a0001c0001t0001g0098 a0001c0001t0001g0099 others(76): Show |
87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.504+3002dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | ||||||
| chr2:168837300 | C | CTT | 27 | a0001c0002t0002g0004 a0001c0002t0002g0157 a0001c0002t0002g0159 others(24): Show |
33 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.504+3001_504+3002d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | ||||||
| chr2:168837300 | CT | C | 16 | a0001c0001t0001g0112 a0001c0001t0001g0256 a0001c0001t0001g0257 others(13): Show |
16 | HG01496.hp2 HG02886.hp2 HG02896.hp1 others(13): Show |
intron_variant | MODIFIER | c.504+3002delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168837300 | ||||||
| chr2:168837371 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.504+3046G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837371 | |||||||
| chr2:168837372 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+3047C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837372 | |||||||
| chr2:168837378 | C | T | 36 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0075 others(33): Show |
37 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.504+3053C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837378 | |||||||
| chr2:168837414 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+3089A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837414 | |||||||
| chr2:168837530 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.504+3205C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837530 | |||||||
| chr2:168837552 | G | A | 1 | a0001c0002t0002g0293 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.504+3227G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837552 | |||||||
| chr2:168837601 | G | A | 1 | a0003c0006t0001g0262 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.504+3276G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837601 | |||||||
| chr2:168837673 | T | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+3348T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837673 | |||||||
| chr2:168837784 | C | T | 14 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0005t0003g0041 others(11): Show |
14 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+3459C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837784 | |||||||
| chr2:168837867 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.504+3542A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837867 | |||||||
| chr2:168837921 | G | C | 64 | a0001c0001t0001g0200 a0001c0001t0002g0266 a0001c0001t0002g0269 others(61): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+3596G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837921 | |||||||
| chr2:168837951 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.504+3626T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168837951 | |||||||
| chr2:168838221 | A | C | 1 | a0001c0001t0001g0014 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.504+3896A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838221 | |||||||
| chr2:168838250 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.504+3925C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838250 | |||||||
| chr2:168838415 | T | G | 1 | a0001c0002t0002g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.504+4090T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838415 | |||||||
| chr2:168838486 | C | T | 9 | a0001c0009t0001g0248 a0003c0006t0001g0006 a0003c0006t0001g0262 others(6): Show |
11 | HG01261.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.504+4161C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838486 | |||||||
| chr2:168838521 | C | T | 64 | a0001c0001t0001g0200 a0001c0001t0001g0265 a0001c0001t0002g0266 others(61): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.504+4196C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838521 | |||||||
| chr2:168838529 | C | A | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+4204C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838529 | |||||||
| chr2:168838529 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.504+4204C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838529 | |||||||
| chr2:168838573 | A | G | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.504+4248A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838573 | |||||||
| chr2:168838603 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(118): Show |
132 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.504+4278G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838603 | |||||||
| chr2:168838606 | A | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0005t0003g0041 others(12): Show |
15 | HG01123.hp1 HG01261.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.504+4281A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838606 | |||||||
| chr2:168838686 | G | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(190): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.505-4306G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838686 | |||||||
| chr2:168838786 | A | ACT | 3 | a0003c0006t0001g0006 a0003c0006t0001g0263 a0003c0013t0003g0264 |
5 | HG01261.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-4203_505-4202d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168838786 | ||||||
| chr2:168838789 | C | CT | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(178): Show |
194 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.505-4188dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168838789 | ||||||
| chr2:168838789 | C | T | 3 | a0001c0004t0002g0252 a0001c0009t0001g0248 a0005c0014t0001g0223 |
3 | HG03041.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.505-4203C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168838789 | |||||||
| chr2:168839020 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(188): Show |
206 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.505-3972G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839020 | |||||||
| chr2:168839048 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.505-3944G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839048 | |||||||
| chr2:168839065 | G | A | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG02027.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-3927G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839065 | |||||||
| chr2:168839141 | C | G | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-3851C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839141 | |||||||
| chr2:168839184 | G | T | 2 | a0001c0010t0001g0055 a0001c0010t0001g0056 |
2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.505-3808G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839184 | |||||||
| chr2:168839253 | C | G | 1 | a0001c0001t0002g0092 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.505-3739C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839253 | |||||||
| chr2:168839448 | G | C | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.505-3544G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839448 | |||||||
| chr2:168839540 | A | G | 1 | a0001c0005t0003g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.505-3452A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839540 | |||||||
| chr2:168839569 | A | G | 1 | a0001c0004t0002g0192 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.505-3423A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839569 | |||||||
| chr2:168839680 | G | T | 3 | a0001c0005t0003g0024 a0001c0010t0001g0055 a0001c0010t0001g0056 |
3 | HG02809.hp1 HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.505-3312G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839680 | |||||||
| chr2:168839695 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0004g0204 a0001c0001t0004g0206 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-3297C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839695 | |||||||
| chr2:168839813 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.505-3179G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839813 | |||||||
| chr2:168839840 | C | T | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-3152C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839840 | |||||||
| chr2:168839884 | C | CA | 46 | a0001c0001t0001g0075 a0001c0001t0001g0081 a0001c0001t0001g0090 others(43): Show |
47 | HG00621.hp2 HG00673.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.505-3091dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | ||||||
| chr2:168839884 | C | CAA | 17 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0114 others(14): Show |
17 | HG00423.hp1 HG01261.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.505-3092_505-3091d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | ||||||
| chr2:168839884 | C | CAAA | 12 | a0001c0001t0001g0187 a0001c0001t0001g0256 a0001c0001t0001g0257 others(9): Show |
12 | HG01123.hp1 HG01496.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.505-3093_505-3091d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839884 | ||||||
| chr2:168839900 | A | T | 1 | a0002c0003t0001g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.505-3092A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839900 | |||||||
| chr2:168839901 | AT | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0091 others(23): Show |
26 | HG01168.hp2 HG01884.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.505-3090delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839901 | |||||||
| chr2:168839901 | ATAT | A | 14 | a0001c0001t0002g0269 a0001c0002t0002g0171 a0001c0002t0002g0194 others(11): Show |
16 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.505-3090_505-3088d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839901 | |||||||
| chr2:168839902 | T | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(227): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.505-3090T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839902 | |||||||
| chr2:168839904 | T | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(209): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.505-3088T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839904 | |||||||
| chr2:168839906 | T | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(197): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.505-3086T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839906 | |||||||
| chr2:168839908 | T | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(179): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.505-3084T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839908 | |||||||
| chr2:168839910 | T | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(172): Show |
189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.505-3082T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839910 | |||||||
| chr2:168839912 | T | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.505-3080T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839912 | |||||||
| chr2:168839914 | T | A | 22 | a0001c0001t0001g0054 a0001c0001t0001g0147 a0001c0001t0001g0165 others(19): Show |
23 | HG00735.hp1 HG01167.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.505-3078T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839914 | |||||||
| chr2:168839921 | A | G | 1 | a0001c0007t0001g0201 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.505-3071A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839921 | |||||||
| chr2:168839921 | ATG | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
21 | HG01175.hp1 HG01884.hp2 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-3053_505-3052d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839921 | ||||||
| chr2:168839921 | ATGTG | A | 45 | a0001c0001t0001g0200 a0001c0002t0002g0003 a0001c0002t0002g0004 others(42): Show |
52 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.505-3055_505-3052d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168839921 | ||||||
| chr2:168839923 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.505-3069G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839923 | |||||||
| chr2:168839925 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(219): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.505-3067G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839925 | |||||||
| chr2:168839927 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(195): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.505-3065G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839927 | |||||||
| chr2:168839929 | G | A | 2 | a0003c0006t0001g0006 a0003c0006t0001g0263 |
4 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-3063G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168839929 | |||||||
| chr2:168840245 | T | C | 1 | a0001c0012t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.505-2747T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840245 | |||||||
| chr2:168840337 | G | A | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-2655G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840337 | |||||||
| chr2:168840432 | A | G | 10 | a0001c0001t0001g0062 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-2560A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840432 | |||||||
| chr2:168840455 | C | G | 101 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0043 others(98): Show |
105 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.505-2537C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840455 | |||||||
| chr2:168840462 | G | A | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-2530G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840462 | |||||||
| chr2:168840466 | C | T | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-2526C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840466 | |||||||
| chr2:168840529 | C | CAA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0155 others(3): Show |
6 | HG00733.hp1 HG02109.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2442_505-2441d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | ||||||
| chr2:168840529 | C | CAAA | 9 | a0001c0001t0001g0187 a0001c0001t0001g0256 a0001c0005t0003g0041 others(6): Show |
9 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-2443_505-2441d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | ||||||
| chr2:168840529 | CA | C | 92 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(89): Show |
96 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.505-2441delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | ||||||
| chr2:168840529 | CAA | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(138): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.505-2442_505-2441d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840529 | ||||||
| chr2:168840540 | A | C | 3 | a0001c0001t0001g0294 a0002c0003t0001g0240 a0002c0003t0001g0241 |
3 | HG02647.hp1 NA18967.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.505-2452A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840540 | |||||||
| chr2:168840541 | A | C | 62 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(59): Show |
66 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.505-2451A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840541 | |||||||
| chr2:168840543 | A | C | 2 | a0001c0004t0002g0191 a0001c0004t0002g0227 |
2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.505-2449A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840543 | |||||||
| chr2:168840546 | A | AAC | 6 | a0001c0001t0001g0203 a0001c0001t0004g0204 a0001c0001t0004g0206 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-2445_505-2444i others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168840546 | ||||||
| chr2:168840546 | A | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-2446A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840546 | |||||||
| chr2:168840552 | C | A | 3 | a0001c0001t0001g0043 a0001c0005t0003g0042 a0001c0005t0003g0044 |
3 | HG02109.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.505-2440C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840552 | |||||||
| chr2:168840572 | G | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0077 others(14): Show |
21 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.505-2420G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840572 | |||||||
| chr2:168840716 | G | A | 8 | a0001c0001t0001g0062 a0001c0001t0002g0028 a0001c0001t0002g0029 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-2276G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840716 | |||||||
| chr2:168840800 | T | C | 2 | a0003c0006t0001g0295 a0003c0006t0001g0296 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.505-2192T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840800 | |||||||
| chr2:168840826 | C | T | 2 | a0003c0006t0001g0006 a0003c0006t0001g0263 |
4 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-2166C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840826 | |||||||
| chr2:168840918 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.505-2074T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840918 | |||||||
| chr2:168840945 | T | G | 8 | a0001c0001t0002g0025 a0001c0005t0003g0007 a0001c0005t0003g0050 others(5): Show |
9 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.505-2047T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840945 | |||||||
| chr2:168840985 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.505-2007G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168840985 | |||||||
| chr2:168841023 | T | C | 64 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(61): Show |
68 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.505-1969T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841023 | |||||||
| chr2:168841040 | C | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(21): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.505-1952C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841040 | |||||||
| chr2:168841151 | C | T | 19 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0148 others(16): Show |
19 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.505-1841C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841151 | |||||||
| chr2:168841235 | C | CA | 22 | a0001c0002t0002g0157 a0001c0002t0002g0162 a0001c0002t0002g0166 others(19): Show |
26 | HG00099.hp1 HG00323.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.505-1731dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | C | CAA | 8 | a0001c0001t0001g0062 a0001c0001t0002g0028 a0001c0001t0002g0057 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-1732_505-1731d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | C | CAAAAAAA others(8): Show |
2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.505-1745_505-1731d others(17): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | CAAAAAAA | C | 17 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0148 others(14): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.505-1737_505-1731d others(9): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
6 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.505-1738_505-1731d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | CAAAAAAA others(2): Show |
C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0249 a0001c0001t0001g0261 others(37): Show |
43 | HG00423.hp1 HG00673.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.505-1739_505-1731d others(11): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0274 a0003c0006t0002g0254 |
2 | HG02976.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.505-1742_505-1731d others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841235 | CAAAAAAA others(6): Show |
C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(129): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.505-1743_505-1731d others(15): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841235 | ||||||
| chr2:168841293 | AATAT | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(195): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.505-1689_505-1686d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841293 | ||||||
| chr2:168841301 | T | G | 1 | a0001c0010t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.505-1691T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841301 | |||||||
| chr2:168841403 | GC | G | 3 | a0001c0001t0001g0258 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1586delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 168841403 | ||||||
| chr2:168841452 | A | T | 64 | a0001c0001t0001g0200 a0001c0001t0002g0266 a0001c0001t0002g0269 others(61): Show |
74 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.505-1540A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841452 | |||||||
| chr2:168841559 | C | A | 3 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0180 |
5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-1433C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841559 | |||||||
| chr2:168841573 | T | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1419T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841573 | |||||||
| chr2:168841790 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0261 |
3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-1202T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841790 | |||||||
| chr2:168841869 | A | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(199): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.505-1123A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841869 | |||||||
| chr2:168841883 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.505-1109G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168841883 | |||||||
| chr2:168842106 | G | A | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.505-886G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842106 | |||||||
| chr2:168842446 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0261 |
3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505-546T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842446 | |||||||
| chr2:168842613 | A | G | 1 | a0001c0004t0002g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505-379A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842613 | |||||||
| chr2:168842754 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.505-238A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842754 | |||||||
| chr2:168842821 | T | C | 10 | a0001c0001t0001g0148 a0001c0001t0001g0233 a0001c0001t0002g0031 others(7): Show |
10 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.505-171T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842821 | |||||||
| chr2:168842840 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(128): Show |
140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.505-152G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842840 | |||||||
| chr2:168842866 | A | G | 1 | a0001c0005t0003g0087 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.505-126A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842866 | |||||||
| chr2:168842928 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.505-64A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 7/15 | chr2 | 168842928 | |||||||
| chr2:168843200 | A | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0058 others(22): Show |
28 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.630+83A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843200 | |||||||
| chr2:168843280 | C | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.630+163C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843280 | |||||||
| chr2:168843472 | G | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0030 others(2): Show |
5 | HG01496.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+355G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843472 | |||||||
| chr2:168843491 | C | T | 1 | a0001c0004t0002g0101 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.630+374C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843491 | |||||||
| chr2:168843620 | A | G | 9 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+503A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843620 | |||||||
| chr2:168843665 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+548G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843665 | |||||||
| chr2:168843758 | G | C | 1 | a0001c0004t0002g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.630+641G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843758 | |||||||
| chr2:168843953 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(274): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.630+836T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168843953 | |||||||
| chr2:168844116 | A | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0002g0030 others(2): Show |
5 | HG01496.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+999A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844116 | |||||||
| chr2:168844235 | C | T | 19 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(16): Show |
20 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.630+1118C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844235 | |||||||
| chr2:168844328 | C | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(105): Show |
117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.630+1211C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844328 | |||||||
| chr2:168844393 | T | TA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(103): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.630+1286dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844393 | ||||||
| chr2:168844393 | T | TAA | 100 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0043 others(97): Show |
104 | HG00423.hp1 HG00642.hp2 HG00673.hp2 others(101): Show |
intron_variant | MODIFIER | c.630+1285_630+1286d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844393 | ||||||
| chr2:168844536 | A | T | 10 | a0001c0001t0001g0062 a0001c0001t0002g0028 a0001c0001t0002g0029 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+1419A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844536 | |||||||
| chr2:168844544 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1427A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844544 | |||||||
| chr2:168844684 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.630+1567C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844684 | |||||||
| chr2:168844686 | C | A | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1569C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844686 | |||||||
| chr2:168844686 | C | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(195): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.630+1569C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844686 | |||||||
| chr2:168844729 | G | A | 1 | a0001c0012t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.630+1612G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844729 | |||||||
| chr2:168844729 | G | C | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630+1612G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844729 | |||||||
| chr2:168844845 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1728A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844845 | |||||||
| chr2:168844865 | G | A | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1748G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844865 | |||||||
| chr2:168844875 | G | GA | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(183): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.630+1771dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844875 | ||||||
| chr2:168844875 | G | GAA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0005t0003g0041 others(12): Show |
15 | HG01123.hp1 HG01261.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.630+1770_630+1771d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168844875 | ||||||
| chr2:168844890 | A | G | 1 | a0001c0002t0002g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.630+1773A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844890 | |||||||
| chr2:168844902 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0261 |
3 | HG01891.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.630+1785C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844902 | |||||||
| chr2:168844936 | G | A | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1819G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844936 | |||||||
| chr2:168844940 | A | T | 18 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(15): Show |
18 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+1823A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844940 | |||||||
| chr2:168844950 | A | G | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+1833A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844950 | |||||||
| chr2:168844960 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.630+1843C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844960 | |||||||
| chr2:168844961 | G | A | 1 | a0001c0004t0002g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1844G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168844961 | |||||||
| chr2:168845089 | G | GA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+1978dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845089 | ||||||
| chr2:168845128 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.630+2011G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845128 | |||||||
| chr2:168845129 | G | A | 10 | a0001c0001t0001g0249 a0001c0001t0002g0025 a0001c0005t0003g0007 others(7): Show |
11 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+2012G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845129 | |||||||
| chr2:168845407 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630+2290G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845407 | |||||||
| chr2:168845503 | T | C | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.630+2386T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845503 | |||||||
| chr2:168845527 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(196): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.630+2410A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845527 | |||||||
| chr2:168845580 | C | T | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+2463C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845580 | |||||||
| chr2:168845601 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0103 a0001c0001t0001g0129 |
3 | HG02056.hp1 NA19076.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.630+2484A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845601 | |||||||
| chr2:168845641 | C | T | 18 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(15): Show |
18 | HG00423.hp1 HG00673.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+2524C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845641 | |||||||
| chr2:168845753 | T | C | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.630+2636T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845753 | |||||||
| chr2:168845789 | C | CCTT | 10 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0136 others(7): Show |
10 | HG01358.hp2 HG01884.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.630+2673_630+2675d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845789 | ||||||
| chr2:168845790 | C | CT | 17 | a0001c0001t0002g0076 a0001c0002t0002g0079 a0001c0002t0002g0080 others(14): Show |
17 | HG00673.hp1 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.630+2690dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | ||||||
| chr2:168845790 | C | CTTCT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(131): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | ||||||
| chr2:168845790 | C | CTTCTT | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0043 others(41): Show |
46 | HG01261.hp1 HG01517.hp2 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | ||||||
| chr2:168845790 | C | CTTCTTT | 18 | a0001c0001t0001g0067 a0001c0001t0001g0187 a0001c0001t0002g0025 others(15): Show |
19 | HG00733.hp1 HG01123.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.630+2675_630+2676i others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168845790 | ||||||
| chr2:168845830 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.630+2713A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168845830 | |||||||
| chr2:168846125 | T | C | 1 | a0001c0004t0002g0018 | 2 | HG01070.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.630+3008T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846125 | |||||||
| chr2:168846188 | A | T | 4 | a0002c0003t0001g0015 a0002c0003t0001g0019 a0002c0003t0001g0246 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+3071A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846188 | |||||||
| chr2:168846270 | G | A | 3 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 |
3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.630+3153G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846270 | |||||||
| chr2:168846285 | G | A | 3 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0180 |
5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+3168G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846285 | |||||||
| chr2:168846325 | T | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+3208T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846325 | |||||||
| chr2:168846419 | A | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(136): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.630+3302A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846419 | |||||||
| chr2:168846486 | T | C | 1 | a0001c0002t0002g0159 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.630+3369T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846486 | |||||||
| chr2:168846524 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(145): Show |
157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.630+3407A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846524 | |||||||
| chr2:168846589 | C | A | 7 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(4): Show |
7 | HG02257.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+3472C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846589 | |||||||
| chr2:168846609 | A | G | 36 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0054 others(33): Show |
40 | HG01255.hp2 HG01884.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.630+3492A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846609 | |||||||
| chr2:168846643 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.630+3526A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846643 | |||||||
| chr2:168846714 | TTTTTAAA others(7): Show |
T | 3 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0098 |
3 | NA18962.hp2 NA18977.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.630+3599_630+3612d others(16): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168846714 | ||||||
| chr2:168846850 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.630+3733T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846850 | |||||||
| chr2:168846920 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630+3803C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846920 | |||||||
| chr2:168846972 | G | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(284): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.630+3855G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168846972 | |||||||
| chr2:168847150 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(123): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.631-3934C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847150 | |||||||
| chr2:168847241 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(120): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.631-3843T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847241 | |||||||
| chr2:168847366 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.631-3718C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847366 | |||||||
| chr2:168847386 | T | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(197): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.631-3698T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847386 | |||||||
| chr2:168847403 | GGAGCCTC others(11): Show |
G | 2 | a0001c0001t0001g0147 a0001c0004t0002g0161 |
2 | HG02523.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.631-3668_631-3651d others(20): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168847403 | ||||||
| chr2:168847464 | G | A | 18 | a0001c0001t0001g0200 a0001c0001t0002g0266 a0001c0001t0002g0269 others(15): Show |
21 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.631-3620G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847464 | |||||||
| chr2:168847638 | A | G | 3 | a0001c0002t0002g0169 a0001c0002t0002g0183 a0001c0004t0002g0212 |
3 | HG03669.hp1 HG03834.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.631-3446A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847638 | |||||||
| chr2:168847801 | G | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0187 |
3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-3283G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847801 | |||||||
| chr2:168847823 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.631-3261T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847823 | |||||||
| chr2:168847906 | T | C | 1 | a0001c0002t0002g0171 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.631-3178T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847906 | |||||||
| chr2:168847977 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(93): Show |
105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-3107T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168847977 | |||||||
| chr2:168848244 | T | A | 17 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0052 others(14): Show |
17 | HG00642.hp2 HG00735.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.631-2840T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848244 | |||||||
| chr2:168848333 | T | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-2751T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848333 | |||||||
| chr2:168848336 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0155 others(2): Show |
5 | HG00733.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-2748C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848336 | |||||||
| chr2:168848395 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0187 |
3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-2689C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848395 | |||||||
| chr2:168848430 | G | A | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-2654G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848430 | |||||||
| chr2:168848527 | T | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(93): Show |
105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-2557T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848527 | |||||||
| chr2:168848560 | CA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(93): Show |
105 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.631-2518delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168848560 | ||||||
| chr2:168848594 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(118): Show |
130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.631-2490A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848594 | |||||||
| chr2:168848806 | T | C | 47 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(44): Show |
50 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(47): Show |
intron_variant | MODIFIER | c.631-2278T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848806 | |||||||
| chr2:168848819 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.631-2265C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848819 | |||||||
| chr2:168848865 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.631-2219T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848865 | |||||||
| chr2:168848867 | G | A | 6 | a0001c0001t0001g0062 a0003c0006t0001g0262 a0003c0006t0001g0295 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-2217G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848867 | |||||||
| chr2:168848876 | T | C | 6 | a0001c0001t0001g0062 a0003c0006t0001g0262 a0003c0006t0001g0295 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-2208T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168848876 | |||||||
| chr2:168849054 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-2030C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849054 | |||||||
| chr2:168849059 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0187 |
3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-2025C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849059 | |||||||
| chr2:168849165 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.631-1919C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849165 | |||||||
| chr2:168849203 | C | T | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.631-1881C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849203 | |||||||
| chr2:168849365 | C | CT | 6 | a0001c0001t0001g0062 a0003c0006t0001g0262 a0003c0006t0001g0295 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-1711dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849365 | ||||||
| chr2:168849372 | T | C | 1 | a0001c0002t0002g0157 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.631-1712T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849372 | |||||||
| chr2:168849558 | G | A | 3 | a0001c0001t0001g0043 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-1526G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849558 | |||||||
| chr2:168849569 | T | C | 131 | a0001c0001t0001g0011 a0001c0001t0001g0054 a0001c0001t0001g0058 others(128): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.631-1515T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849569 | |||||||
| chr2:168849646 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0187 |
3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-1438G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849646 | |||||||
| chr2:168849670 | C | CA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(99): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.631-1395dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | ||||||
| chr2:168849670 | C | CAA | 28 | a0001c0001t0001g0043 a0001c0001t0001g0066 a0001c0001t0001g0102 others(25): Show |
30 | HG00423.hp1 HG01109.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.631-1396_631-1395d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | ||||||
| chr2:168849670 | C | CAAA | 121 | a0001c0001t0001g0011 a0001c0001t0001g0054 a0001c0001t0001g0058 others(118): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.631-1397_631-1395d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | ||||||
| chr2:168849670 | C | CAAAA | 13 | a0001c0001t0001g0156 a0001c0001t0001g0258 a0001c0001t0002g0025 others(10): Show |
14 | HG00621.hp1 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.631-1398_631-1395d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849670 | ||||||
| chr2:168849748 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.631-1336G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849748 | |||||||
| chr2:168849905 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
15 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.631-1179G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849905 | |||||||
| chr2:168849918 | A | ATTTTG | 30 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0089 others(27): Show |
30 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849918 | ||||||
| chr2:168849918 | A | ATTTTGT | 72 | a0001c0001t0002g0266 a0001c0001t0002g0269 a0001c0002t0002g0003 others(69): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849918 | ||||||
| chr2:168849919 | T | TTTTG | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(149): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.631-1162_631-1161i others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168849919 | ||||||
| chr2:168849923 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-1161T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168849923 | |||||||
| chr2:168850024 | TG | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-1059delG | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850024 | |||||||
| chr2:168850176 | G | A | 3 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 |
3 | HG02572.hp1 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.631-908G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850176 | |||||||
| chr2:168850193 | A | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-891A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850193 | |||||||
| chr2:168850557 | A | G | 2 | a0001c0005t0003g0250 a0001c0005t0003g0251 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.631-527A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850557 | |||||||
| chr2:168850596 | A | AT | 16 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0126 others(13): Show |
16 | HG00438.hp1 HG00621.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.631-469dupT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | ||||||
| chr2:168850596 | AT | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-469delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | ||||||
| chr2:168850596 | ATT | A | 17 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(14): Show |
18 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.631-470_631-469del others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850596 | ||||||
| chr2:168850597 | T | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0187 |
3 | HG01123.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.631-487T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850597 | |||||||
| chr2:168850638 | C | T | 1 | a0001c0002t0002g0287 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.631-446C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850638 | |||||||
| chr2:168850699 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.631-385G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850699 | |||||||
| chr2:168850752 | A | AAATTCTC others(3): Show |
1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-318_631-309dup others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850752 | ||||||
| chr2:168850752 | AAATTCTC others(3): Show |
A | 77 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0155 others(74): Show |
87 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.631-318_631-309del others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 168850752 | ||||||
| chr2:168850812 | T | C | 1 | a0001c0005t0003g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.631-272T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850812 | |||||||
| chr2:168850918 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(111): Show |
123 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.631-166C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850918 | |||||||
| chr2:168850945 | T | C | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.631-139T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168850945 | |||||||
| chr2:168851042 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(113): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.631-42A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168851042 | |||||||
| chr2:168851067 | A | G | 5 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.631-17A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 8/15 | chr2 | 168851067 | |||||||
| chr2:168851267 | T | C | 2 | a0001c0005t0003g0042 a0001c0005t0003g0044 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.730-12T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 9/15 | chr2 | 168851267 | |||||||
| chr2:168851478 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.855+74T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851478 | |||||||
| chr2:168851503 | A | C | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.855+99A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851503 | |||||||
| chr2:168851537 | A | T | 3 | a0001c0001t0001g0043 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+133A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851537 | |||||||
| chr2:168851643 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.855+239C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851643 | |||||||
| chr2:168851687 | C | G | 1 | a0001c0005t0003g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.855+283C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851687 | |||||||
| chr2:168851710 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
19 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.855+306C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851710 | |||||||
| chr2:168851759 | C | T | 1 | a0002c0003t0001g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.855+355C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851759 | |||||||
| chr2:168851798 | A | T | 21 | a0001c0001t0002g0025 a0001c0001t0002g0030 a0001c0001t0002g0031 others(18): Show |
21 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.855+394A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851798 | |||||||
| chr2:168851812 | A | G | 1 | a0001c0005t0003g0141 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.855+408A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851812 | |||||||
| chr2:168851864 | C | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
19 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.855+460C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851864 | |||||||
| chr2:168851980 | C | T | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.855+576C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168851980 | |||||||
| chr2:168852374 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.855+970G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852374 | |||||||
| chr2:168852391 | T | C | 2 | a0001c0001t0004g0204 a0001c0001t0004g0206 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.855+987T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852391 | |||||||
| chr2:168852432 | T | C | 3 | a0001c0001t0001g0043 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+1028T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852432 | |||||||
| chr2:168852503 | C | T | 9 | a0001c0005t0003g0007 a0001c0005t0003g0050 a0001c0005t0003g0084 others(6): Show |
10 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.855+1099C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852503 | |||||||
| chr2:168852504 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0261 |
4 | HG01891.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+1100T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852504 | |||||||
| chr2:168852563 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.855+1159C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852563 | |||||||
| chr2:168852594 | C | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(262): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.855+1190C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852594 | |||||||
| chr2:168852687 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(140): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.855+1283C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852687 | |||||||
| chr2:168852954 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0002g0028 a0001c0001t0002g0029 others(6): Show |
11 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.855+1550G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168852954 | |||||||
| chr2:168853172 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.855+1768G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853172 | |||||||
| chr2:168853247 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(112): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.855+1843G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853247 | |||||||
| chr2:168853484 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.856-1868G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853484 | |||||||
| chr2:168853648 | C | T | 2 | a0002c0003t0001g0036 a0002c0003t0001g0037 |
2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.856-1704C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853648 | |||||||
| chr2:168853674 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.856-1678G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853674 | |||||||
| chr2:168853782 | G | A | 2 | a0001c0002t0002g0177 a0001c0002t0002g0182 |
2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.856-1570G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853782 | |||||||
| chr2:168853867 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.856-1485A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853867 | |||||||
| chr2:168853928 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1424C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853928 | |||||||
| chr2:168853943 | C | A | 2 | a0002c0003t0001g0240 a0002c0003t0001g0241 |
2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.856-1409C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168853943 | |||||||
| chr2:168854025 | G | A | 30 | a0001c0005t0003g0007 a0001c0005t0003g0021 a0001c0005t0003g0024 others(27): Show |
32 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.856-1327G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854025 | |||||||
| chr2:168854028 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1324C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854028 | |||||||
| chr2:168854097 | G | A | 77 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0155 others(74): Show |
87 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.856-1255G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854097 | |||||||
| chr2:168854349 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.856-1003C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854349 | |||||||
| chr2:168854390 | C | T | 1 | a0001c0004t0002g0218 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.856-962C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854390 | |||||||
| chr2:168854467 | TC | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-884delC | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854467 | |||||||
| chr2:168854608 | T | G | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-744T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854608 | |||||||
| chr2:168854751 | C | T | 2 | a0002c0003t0001g0009 a0002c0003t0001g0035 |
3 | HG00099.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.856-601C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854751 | |||||||
| chr2:168854794 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(117): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.856-558T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854794 | |||||||
| chr2:168854838 | T | G | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.856-514T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 10/15 | chr2 | 168854838 | |||||||
| chr2:168855486 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+26C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855486 | |||||||
| chr2:168855558 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0155 others(2): Show |
5 | HG00733.hp1 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.964+98G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855558 | |||||||
| chr2:168855566 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.964+106T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855566 | |||||||
| chr2:168855603 | A | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
20 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.964+143A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855603 | |||||||
| chr2:168855605 | C | CA | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(193): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.964+158dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855605 | ||||||
| chr2:168855607 | A | AC | 3 | a0001c0001t0001g0103 a0001c0001t0001g0187 a0001c0001t0001g0253 |
3 | HG01123.hp1 HG02056.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.964+147_964+148ins others(1): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855607 | |||||||
| chr2:168855617 | AAGT | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(9): Show |
13 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.964+160_964+162del others(3): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855617 | ||||||
| chr2:168855638 | C | CA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(196): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.964+194dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | ||||||
| chr2:168855638 | C | CAA | 41 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0187 others(38): Show |
46 | HG00140.hp1 HG00423.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.964+193_964+194dup others(2): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | ||||||
| chr2:168855638 | C | CAAA | 7 | a0001c0001t0001g0294 a0001c0005t0003g0237 a0001c0005t0003g0260 others(4): Show |
7 | HG02074.hp2 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+192_964+194dup others(3): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | ||||||
| chr2:168855638 | C | CAAAA | 25 | a0001c0005t0003g0007 a0001c0005t0003g0021 a0001c0005t0003g0024 others(22): Show |
27 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.964+191_964+194dup others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | ||||||
| chr2:168855638 | CAAAA | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
18 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.964+191_964+194del others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855638 | ||||||
| chr2:168855890 | T | TA | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+431dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168855890 | ||||||
| chr2:168855995 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+535C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168855995 | |||||||
| chr2:168856068 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.964+608C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856068 | |||||||
| chr2:168856076 | A | G | 19 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(16): Show |
20 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.965-614A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856076 | |||||||
| chr2:168856084 | G | A | 58 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(55): Show |
61 | HG00423.hp1 HG01255.hp2 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.965-606G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856084 | |||||||
| chr2:168856086 | T | C | 31 | a0001c0005t0003g0007 a0001c0005t0003g0021 a0001c0005t0003g0024 others(28): Show |
33 | HG01255.hp2 HG01261.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.965-604T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856086 | |||||||
| chr2:168856420 | C | T | 13 | a0002c0003t0001g0022 a0002c0003t0001g0064 a0002c0003t0001g0083 others(10): Show |
14 | NA18945.hp1 NA18949.hp1 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-270C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856420 | |||||||
| chr2:168856537 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.965-153T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | chr2 | 168856537 | |||||||
| chr2:168856574 | T | TA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(146): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.965-105dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 168856574 | ||||||
| chr2:168856823 | G | T | 1 | a0001c0010t0001g0055 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1053+45G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856823 | |||||||
| chr2:168856841 | T | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(17): Show |
21 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(18): Show |
intron_variant | MODIFIER | c.1053+63T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856841 | |||||||
| chr2:168856901 | G | C | 3 | a0001c0001t0001g0043 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1053+123G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168856901 | |||||||
| chr2:168857010 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1053+232G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857010 | |||||||
| chr2:168857068 | G | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+290G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857068 | |||||||
| chr2:168857173 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1053+395C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857173 | |||||||
| chr2:168857299 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1053+521T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857299 | |||||||
| chr2:168857518 | G | C | 1 | a0002c0003t0001g0008 | 2 | HG01928.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1053+740G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857518 | |||||||
| chr2:168857730 | T | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+952T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857730 | |||||||
| chr2:168857840 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(147): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1053+1062T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857840 | |||||||
| chr2:168857881 | T | C | 2 | a0001c0007t0001g0201 a0001c0007t0001g0202 |
2 | HG02074.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1053+1103T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857881 | |||||||
| chr2:168857975 | G | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1053+1197G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168857975 | |||||||
| chr2:168858017 | C | T | 31 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(28): Show |
32 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.1053+1239C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858017 | |||||||
| chr2:168858072 | C | T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0272 a0001c0001t0001g0273 others(6): Show |
9 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1053+1294C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858072 | |||||||
| chr2:168858167 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1054-1345A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858167 | |||||||
| chr2:168858172 | T | G | 1 | a0001c0002t0002g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1054-1340T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858172 | |||||||
| chr2:168858379 | T | C | 1 | a0001c0004t0002g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1054-1133T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858379 | |||||||
| chr2:168858383 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(116): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1054-1129T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858383 | |||||||
| chr2:168858522 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1054-990G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858522 | |||||||
| chr2:168858817 | G | A | 5 | a0003c0006t0001g0262 a0003c0006t0001g0295 a0003c0006t0001g0296 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-695G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168858817 | |||||||
| chr2:168859097 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1054-415C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859097 | |||||||
| chr2:168859100 | C | T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0272 a0001c0001t0001g0273 others(6): Show |
9 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1054-412C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859100 | |||||||
| chr2:168859176 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(117): Show |
129 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1054-336A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859176 | |||||||
| chr2:168859192 | A | C | 15 | a0001c0001t0002g0025 a0001c0001t0002g0030 a0001c0001t0002g0031 others(12): Show |
15 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-320A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859192 | |||||||
| chr2:168859195 | T | C | 1 | a0001c0002t0002g0213 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1054-317T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859195 | |||||||
| chr2:168859207 | T | A | 1 | a0001c0009t0001g0255 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1054-305T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859207 | |||||||
| chr2:168859357 | AT | A | 31 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(28): Show |
32 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.1054-146delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 168859357 | ||||||
| chr2:168859371 | C | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(29): Show |
33 | HG00423.hp1 HG01123.hp1 HG01943.hp2 others(30): Show |
intron_variant | MODIFIER | c.1054-141C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 12/15 | chr2 | 168859371 | |||||||
| chr2:168859762 | TAAG | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179+130_1179+132d others(5): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168859762 | ||||||
| chr2:168859823 | A | G | 1 | a0002c0003t0001g0026 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1179+186A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859823 | |||||||
| chr2:168859876 | T | C | 1 | a0001c0002t0002g0016 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1179+239T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859876 | |||||||
| chr2:168859906 | C | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+269C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168859906 | |||||||
| chr2:168860008 | T | G | 3 | a0001c0001t0001g0043 a0003c0006t0001g0006 a0003c0006t0001g0263 |
5 | HG01261.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+371T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860008 | |||||||
| chr2:168860151 | A | G | 3 | a0001c0002t0002g0195 a0001c0002t0002g0198 a0001c0002t0002g0220 |
3 | HG00621.hp1 HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1179+514A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860151 | |||||||
| chr2:168860182 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179+545C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860182 | |||||||
| chr2:168860222 | T | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
23 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1180-573T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860222 | |||||||
| chr2:168860279 | G | T | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180-516G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860279 | |||||||
| chr2:168860396 | C | T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG00423.hp2 NA18960.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1180-399C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860396 | |||||||
| chr2:168860446 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1180-349G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860446 | |||||||
| chr2:168860488 | C | T | 16 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.1180-307C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860488 | |||||||
| chr2:168860504 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0261 |
4 | HG01891.hp1 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-291C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860504 | |||||||
| chr2:168860596 | G | A | 1 | a0002c0003t0001g0032 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1180-199G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860596 | |||||||
| chr2:168860613 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1180-182G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860613 | |||||||
| chr2:168860652 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-143C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860652 | |||||||
| chr2:168860669 | T | TA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(150): Show |
166 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1180-114dupA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168860669 | ||||||
| chr2:168860680 | AAGAAAAA others(6): Show |
A | 1 | a0001c0002t0002g0167 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1180-103_1180-91de others(14): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 168860680 | ||||||
| chr2:168860686 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-109A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860686 | |||||||
| chr2:168860689 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1180-106C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 13/15 | chr2 | 168860689 | |||||||
| chr2:168860923 | C | T | 1 | a0001c0002t0002g0287 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1294+14C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168860923 | |||||||
| chr2:168861031 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(180): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1294+122T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861031 | |||||||
| chr2:168861050 | A | T | 1 | a0001c0001t0002g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1294+141A>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861050 | |||||||
| chr2:168861061 | C | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(15): Show |
19 | HG02055.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.1294+152C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861061 | |||||||
| chr2:168861114 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1294+205C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861114 | |||||||
| chr2:168861318 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1294+409T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861318 | |||||||
| chr2:168861408 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
8 | HG00558.hp2 HG01257.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1294+499C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861408 | |||||||
| chr2:168861484 | TA | T | 8 | a0001c0001t0001g0249 a0001c0001t0001g0258 a0001c0001t0001g0274 others(5): Show |
8 | NA18961.hp1 NA18994.hp1 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-462delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 168861484 | ||||||
| chr2:168861590 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1295-370G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861590 | |||||||
| chr2:168861791 | G | A | 63 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(60): Show |
66 | HG00423.hp1 HG01123.hp1 HG01255.hp2 others(63): Show |
intron_variant | MODIFIER | c.1295-169G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 14/15 | chr2 | 168861791 | |||||||
| chr2:168862123 | G | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1384+74G>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862123 | |||||||
| chr2:168862127 | G | A | 4 | a0001c0005t0003g0021 a0001c0005t0003g0072 a0001c0005t0003g0236 others(1): Show |
5 | HG01255.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+78G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862127 | |||||||
| chr2:168862367 | T | C | 3 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0180 |
5 | HG03490.hp2 HG03492.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384+318T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862367 | |||||||
| chr2:168862385 | C | CACAAG | 3 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0132 |
3 | HG00140.hp2 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1384+338_1384+342d others(7): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862385 | ||||||
| chr2:168862392 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(225): Show |
251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1384+343T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862392 | |||||||
| chr2:168862471 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1384+422A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862471 | |||||||
| chr2:168862543 | TGTAA | T | 92 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0029 others(89): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1384+501_1384+504d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862543 | ||||||
| chr2:168862554 | G | T | 1 | a0001c0004t0002g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1384+505G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862554 | |||||||
| chr2:168862569 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1384+520T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862569 | |||||||
| chr2:168862756 | C | CTTCTTTA others(1): Show |
95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(92): Show |
103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1384+708_1384+715d others(10): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168862756 | ||||||
| chr2:168862819 | C | T | 8 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0289 others(5): Show |
8 | HG00423.hp1 HG01943.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1384+770C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862819 | |||||||
| chr2:168862852 | G | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0230 a0001c0001t0002g0266 |
3 | HG00642.hp2 HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1384+803G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862852 | |||||||
| chr2:168862990 | T | G | 92 | a0001c0001t0002g0025 a0001c0001t0002g0028 a0001c0001t0002g0029 others(89): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1384+941T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168862990 | |||||||
| chr2:168863027 | AAGAC | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1384+984_1384+987d others(6): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863027 | ||||||
| chr2:168863129 | G | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1384+1080G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863129 | |||||||
| chr2:168863142 | C | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0249 a0001c0010t0001g0055 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1384+1093C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863142 | |||||||
| chr2:168863193 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(238): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.1384+1144C>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863193 | |||||||
| chr2:168863296 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(263): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1384+1247A>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863296 | |||||||
| chr2:168863363 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(241): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1384+1314T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863363 | |||||||
| chr2:168863432 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1384+1383G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863432 | |||||||
| chr2:168863441 | T | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(239): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1384+1392T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863441 | |||||||
| chr2:168863472 | A | C | 1 | a0001c0007t0001g0078 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1385-1362A>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863472 | |||||||
| chr2:168863485 | G | A | 1 | a0001c0004t0002g0045 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1385-1349G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863485 | |||||||
| chr2:168863569 | T | A | 6 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG02055.hp1 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1385-1265T>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863569 | |||||||
| chr2:168863660 | G | T | 6 | a0001c0001t0001g0062 a0003c0006t0001g0262 a0003c0006t0001g0295 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1385-1174G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863660 | |||||||
| chr2:168863669 | TGTGA | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(260): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1385-1158_1385-115 others(8): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863669 | ||||||
| chr2:168863705 | G | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1385-1129G>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863705 | |||||||
| chr2:168863903 | C | T | 1 | a0001c0007t0001g0202 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1385-931C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863903 | |||||||
| chr2:168863917 | A | ATT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0155 others(3): Show |
6 | HG00733.hp1 HG02818.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1385-907_1385-906d others(4): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863917 | ||||||
| chr2:168863921 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1385-913T>C | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863921 | |||||||
| chr2:168863979 | TAGCTCAC others(50): Show |
T | 2 | a0001c0002t0002g0195 a0001c0002t0002g0220 |
2 | HG00621.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1385-796_1385-740d others(59): Show |
NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168863979 | ||||||
| chr2:168863997 | G | A | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0057 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1385-837G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168863997 | |||||||
| chr2:168864226 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(10): Show |
14 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1385-608C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864226 | |||||||
| chr2:168864229 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0187 |
2 | HG01123.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1385-605G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864229 | |||||||
| chr2:168864285 | GT | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(258): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1385-538delT | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168864285 | ||||||
| chr2:168864430 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1385-404C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864430 | |||||||
| chr2:168864506 | GA | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(236): Show |
262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.1385-325delA | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 168864506 | ||||||
| chr2:168864530 | C | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(91): Show |
103 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1385-304C>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864530 | |||||||
| chr2:168864564 | C | T | 1 | a0003c0006t0002g0254 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1385-270C>T | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864564 | |||||||
| chr2:168864565 | G | A | 1 | a0001c0012t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1385-269G>A | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864565 | |||||||
| chr2:168864640 | T | G | 40 | a0001c0001t0001g0187 a0001c0001t0001g0272 a0001c0001t0001g0273 others(37): Show |
42 | HG00423.hp1 HG01123.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1385-194T>G | NOSTRIN | ENSG00000163072.16 | transcript | ENST00000317647.12 | protein_coding | 15/15 | chr2 | 168864640 |