Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29959 |
| ensemblid | ENSG00000115216.14 |
| hgncid | 7993 |
| symbol | NRBP1 |
| name | nuclear receptor binding protein 1 |
| refseq_nuc | NM_013392.4 |
| refseq_prot | NP_037524.1 |
| ensembl_nuc | ENST00000379852.8 |
| ensembl_prot | ENSP00000369181.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 27428631 |
| end | 27442259 |
| strand | + |
| ver | v1.2 |
| region | chr2:27428631-27442259 |
| region5000 | chr2:27423631-27447259 |
| regionname0 | NRBP1_chr2_27428631_27442259 |
| regionname5000 | NRBP1_chr2_27423631_27447259 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 535 | 267 | 81 | 55 | 82 | 11 | 36 | 63 | NRBP1_chr2_27423631_27447259 | NRBP1 | MSEGE others(530): Show |
chr2 | 27423631 | 27447259 |
| a0002 | 0/0 | 535 | 6 | 3 | 3 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | MSEGE others(530): Show |
chr2 | 27423631 | 27447259 |
| a0003 | 0/0 | 331 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | MSEGE others(326): Show |
chr2 | 27423631 | 27447259 |
| a0004 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | MSEGE others(530): Show |
chr2 | 27423631 | 27447259 |
| a0005 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | MSEGE others(530): Show |
chr2 | 27423631 | 27447259 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1605 | 265 | 81 | 55 | 80 | 11 | 36 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1600): Show |
chr2 | 27423631 | 27447259 | ||
| a0001c0003 | 0/0 | 1605 | 2 | 0 | 0 | 2 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1600): Show |
chr2 | 27423631 | 27447259 | ||
| a0002c0002 | 0/0 | 1605 | 6 | 3 | 3 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1600): Show |
chr2 | 27423631 | 27447259 | ||
| a0003c0006 | 0/0 | 1615 | 1 | 0 | 0 | 0 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1610): Show |
chr2 | 27423631 | 27447259 | ||
| a0004c0004 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1600): Show |
chr2 | 27423631 | 27447259 | ||
| a0005c0005 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | ATGTC others(1600): Show |
chr2 | 27423631 | 27447259 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2176 | 252 | 71 | 54 | 78 | 11 | 36 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0002 | 0/0 | 2176 | 3 | 3 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0003 | 0/0 | 2176 | 3 | 3 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0004 | 0/0 | 2176 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0005 | 0/0 | 2176 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0006 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0007 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0008 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0001t0009 | 0/0 | 2176 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0001c0003t0001 | 0/0 | 2176 | 2 | 0 | 0 | 2 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0002c0002t0001 | 0/0 | 2176 | 6 | 3 | 3 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0003c0006t0001 | 0/0 | 2186 | 1 | 0 | 0 | 0 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2181): Show |
chr2 | 27423631 | 27447259 |
| a0004c0004t0001 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| a0005c0005t0001 | 0/0 | 2176 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | GGTTG others(2171): Show |
chr2 | 27423631 | 27447259 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 37 | 0 | 14 | 14 | 2 | 6 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0002 | 0/0 | 37 | 4 | 5 | 21 | 1 | 6 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0003 | 0/0 | 18 | 7 | 4 | 0 | 4 | 3 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0004 | 0/0 | 11 | 3 | 2 | 5 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 4 | 0 | 4 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0007 | 1/0 | 6 | 0 | 1 | 4 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0002c0002t0001g0005 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0003c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0004c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| a0005c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01517 | hp2 | a0003 | c0006 | t0001 | g0069 | EUR | IBS | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02080 | hp2 | a0004 | c0004 | t0001 | g0083 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0005 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18990 | hp1 | a0005 | c0005 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | USA | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | USA | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | NRBP1_chr2_27423631_27447259 | NRBP1 | chr2 | 27423631 | 27447259 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27428729 | G | A | 1 | a0001 | 1 | HG01496.hp2 | splice_region_variant | LOW | c.-23G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/18 | chr2 | 27428729 | |||||||
| chr2:27439776 | A | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.914A>G | p.Gln305Arg | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1035/2176 | 914/1608 | 305/535 | chr2 | 27439776 | |||
| chr2:27439777 | A | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.915A>C | p.Gln305His | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1036/2176 | 915/1608 | 305/535 | chr2 | 27439777 | |||
| chr2:27439779 | A | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.917A>G | p.Lys306Arg | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1038/2176 | 917/1608 | 306/535 | chr2 | 27439779 | |||
| chr2:27439781 | T | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.919T>C | p.Cys307Arg | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1040/2176 | 919/1608 | 307/535 | chr2 | 27439781 | |||
| chr2:27439782 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.920G>A | p.Cys307Tyr | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1041/2176 | 920/1608 | 307/535 | chr2 | 27439782 | |||
| chr2:27439786 | G | GGCAAGCC others(3): Show |
1 | a0003 | 1 | HG01517.hp2 | frameshift_variant | HIGH | c.924_925insGCAAGCCC others(2): Show |
p.Gln309fs | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1046/2176 | 925/1608 | 309/535 | chr2 | 27439786 | |||
| chr2:27439791 | C | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.929C>G | p.Ser310Cys | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1050/2176 | 929/1608 | 310/535 | chr2 | 27439791 | |||
| chr2:27439794 | A | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.932A>T | p.Glu311Val | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1053/2176 | 932/1608 | 311/535 | chr2 | 27439794 | |||
| chr2:27439795 | G | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.933G>T | p.Glu311Asp | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1054/2176 | 933/1608 | 311/535 | chr2 | 27439795 | |||
| chr2:27439797 | C | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.935C>A | p.Pro312His | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1056/2176 | 935/1608 | 312/535 | chr2 | 27439797 | |||
| chr2:27439800 | C | T | 1 | a0005 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.938C>T | p.Ala313Val | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1059/2176 | 938/1608 | 313/535 | chr2 | 27439800 | |||
| chr2:27439803 | G | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.941G>T | p.Arg314Leu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1062/2176 | 941/1608 | 314/535 | chr2 | 27439803 | |||
| chr2:27439806 | G | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.944G>T | p.Arg315Ile | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1065/2176 | 944/1608 | 315/535 | chr2 | 27439806 | |||
| chr2:27439809 | C | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.947C>T | p.Pro316Leu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1068/2176 | 947/1608 | 316/535 | chr2 | 27439809 | |||
| chr2:27439811 | A | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.949A>T | p.Thr317Ser | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1070/2176 | 949/1608 | 317/535 | chr2 | 27439811 | |||
| chr2:27439818 | G | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.956G>C | p.Arg319Thr | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1077/2176 | 956/1608 | 319/535 | chr2 | 27439818 | |||
| chr2:27439820 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.958G>A | p.Glu320Lys | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1079/2176 | 958/1608 | 320/535 | chr2 | 27439820 | |||
| chr2:27439821 | A | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.959A>G | p.Glu320Gly | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1080/2176 | 959/1608 | 320/535 | chr2 | 27439821 | |||
| chr2:27439835 | C | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.973C>A | p.Pro325Thr | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1094/2176 | 973/1608 | 325/535 | chr2 | 27439835 | |||
| chr2:27439836 | C | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.974C>T | p.Pro325Leu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1095/2176 | 974/1608 | 325/535 | chr2 | 27439836 | |||
| chr2:27439847 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.985G>A | p.Glu329Lys | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1106/2176 | 985/1608 | 329/535 | chr2 | 27439847 | |||
| chr2:27439856 | T | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.994T>C | p.Ser332Pro | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1115/2176 | 994/1608 | 332/535 | chr2 | 27439856 | |||
| chr2:27439857 | C | A | 1 | a0003 | 1 | HG01517.hp2 | stop_gained | HIGH | c.995C>A | p.Ser332* | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1116/2176 | 995/1608 | 332/535 | chr2 | 27439857 | |||
| chr2:27439868 | C | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1006C>G | p.Leu336Val | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1127/2176 | 1006/1608 | 336/535 | chr2 | 27439868 | |||
| chr2:27439869 | T | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1007T>C | p.Leu336Pro | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1128/2176 | 1007/1608 | 336/535 | chr2 | 27439869 | |||
| chr2:27439874 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1012G>A | p.Ala338Thr | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1133/2176 | 1012/1608 | 338/535 | chr2 | 27439874 | |||
| chr2:27439875 | C | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1013C>A | p.Ala338Asp | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1134/2176 | 1013/1608 | 338/535 | chr2 | 27439875 | |||
| chr2:27439879 | C | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1017C>A | p.His339Gln | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1138/2176 | 1017/1608 | 339/535 | chr2 | 27439879 | |||
| chr2:27439886 | G | T | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1024G>T | p.Val342Leu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1145/2176 | 1024/1608 | 342/535 | chr2 | 27439886 | |||
| chr2:27439889 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1027G>A | p.Gly343Arg | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1148/2176 | 1027/1608 | 343/535 | chr2 | 27439889 | |||
| chr2:27439890 | G | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1028G>A | p.Gly343Glu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1149/2176 | 1028/1608 | 343/535 | chr2 | 27439890 | |||
| chr2:27439892 | C | A | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1030C>A | p.His344Asn | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1151/2176 | 1030/1608 | 344/535 | chr2 | 27439892 | |||
| chr2:27439895 | C | G | 1 | a0003 | 1 | HG01517.hp2 | missense_variant | MODERATE | c.1033C>G | p.Gln345Glu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1154/2176 | 1033/1608 | 345/535 | chr2 | 27439895 | |||
| chr2:27439896 | A | C | 1 | a0003 | 1 | HG01517.hp2 | missense_variant&splice_region_variant | MODERATE | c.1034A>C | p.Gln345Pro | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1155/2176 | 1034/1608 | 345/535 | chr2 | 27439896 | |||
| chr2:27440459 | G | A | 1 | a0002 | 6 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
missense_variant | MODERATE | c.1093G>A | p.Val365Ile | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 12/18 | 1214/2176 | 1093/1608 | 365/535 | chr2 | 27440459 | |||
| chr2:27441176 | A | G | 1 | a0004 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1379A>G | p.His460Arg | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 15/18 | 1500/2176 | 1379/1608 | 460/535 | chr2 | 27441176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27436766 | T | C | 1 | a0001c0003 | 2 | NA18963.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.675T>C | p.Thr225Thr | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 8/18 | 796/2176 | 675/1608 | 225/535 | chr2 | 27436766 | |||
| chr2:27439783 | C | T | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.921C>T | p.Cys307Cys | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1042/2176 | 921/1608 | 307/535 | chr2 | 27439783 | |||
| chr2:27439810 | A | C | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.948A>C | p.Pro316Pro | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1069/2176 | 948/1608 | 316/535 | chr2 | 27439810 | |||
| chr2:27439822 | A | G | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.960A>G | p.Glu320Glu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1081/2176 | 960/1608 | 320/535 | chr2 | 27439822 | |||
| chr2:27439849 | A | G | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.987A>G | p.Glu329Glu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1108/2176 | 987/1608 | 329/535 | chr2 | 27439849 | |||
| chr2:27439855 | C | T | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.993C>T | p.Pro331Pro | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1114/2176 | 993/1608 | 331/535 | chr2 | 27439855 | |||
| chr2:27439867 | C | T | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1005C>T | p.Leu335Leu | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1126/2176 | 1005/1608 | 335/535 | chr2 | 27439867 | |||
| chr2:27439876 | C | A | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1014C>A | p.Ala338Ala | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1135/2176 | 1014/1608 | 338/535 | chr2 | 27439876 | |||
| chr2:27439885 | T | A | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1023T>A | p.Ile341Ile | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1144/2176 | 1023/1608 | 341/535 | chr2 | 27439885 | |||
| chr2:27439894 | C | T | 1 | a0003c0006 | 1 | HG01517.hp2 | synonymous_variant | LOW | c.1032C>T | p.His344His | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/18 | 1153/2176 | 1032/1608 | 344/535 | chr2 | 27439894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27428670 | A | G | 1 | a0001c0001t0009 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/18 | 4604 | chr2 | 27428670 | ||||||
| chr2:27441917 | C | T | 1 | a0001c0001t0004 | 2 | HG03041.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*105C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 105 | chr2 | 27441917 | ||||||
| chr2:27441941 | G | T | 1 | a0001c0001t0003 | 3 | HG02622.hp1 HG03540.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*129G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 129 | chr2 | 27441941 | ||||||
| chr2:27442061 | T | C | 1 | a0001c0001t0002 | 3 | HG02145.hp1 HG02451.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*249T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 249 | chr2 | 27442061 | ||||||
| chr2:27442143 | A | G | 1 | a0001c0001t0008 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*331A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 331 | chr2 | 27442143 | ||||||
| chr2:27442162 | C | A | 1 | a0001c0001t0006 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350C>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 350 | chr2 | 27442162 | ||||||
| chr2:27442218 | G | A | 1 | a0001c0001t0007 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 18/18 | 406 | chr2 | 27442218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:27428734 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | HG00609.hp1 NA18957.hp1 NA19000.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-21+3G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27428734 | |||||||
| chr2:27428741 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+10C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27428741 | |||||||
| chr2:27428765 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-21+34A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27428765 | |||||||
| chr2:27428826 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+95T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27428826 | |||||||
| chr2:27428959 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-21+228C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27428959 | |||||||
| chr2:27429060 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0058 |
10 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+329C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429060 | |||||||
| chr2:27429253 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0057 |
3 | HG02257.hp2 HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-21+522A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429253 | |||||||
| chr2:27429286 | G | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-21+555G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429286 | |||||||
| chr2:27429376 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-21+645G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429376 | |||||||
| chr2:27429529 | C | CGAG | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+799_-21+801dup others(3): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 27429529 | ||||||
| chr2:27429684 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-21+953G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429684 | |||||||
| chr2:27429737 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-21+1006G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429737 | |||||||
| chr2:27429887 | T | C | 1 | a0001c0001t0001g0009 | 4 | HG06807.hp2 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+1156T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429887 | |||||||
| chr2:27429921 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-21+1190T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27429921 | |||||||
| chr2:27430052 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-21+1321A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430052 | |||||||
| chr2:27430121 | C | G | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-21+1390C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430121 | |||||||
| chr2:27430304 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-21+1573G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430304 | |||||||
| chr2:27430376 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0026 |
5 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+1645A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430376 | |||||||
| chr2:27430411 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-21+1680T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430411 | |||||||
| chr2:27430469 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+1738C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430469 | |||||||
| chr2:27430469 | CT | C | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG01175.hp1 HG02040.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+1755delT | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 27430469 | ||||||
| chr2:27430478 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0036 others(4): Show |
15 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-21+1747T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430478 | |||||||
| chr2:27430478 | T | TC | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(36): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21+1747_-21+1748i others(3): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430478 | |||||||
| chr2:27430488 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-21+1757A>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430488 | |||||||
| chr2:27430579 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-21+1848G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430579 | |||||||
| chr2:27430686 | T | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0003c0006t0001g0069 |
4 | HG01516.hp2 HG01517.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+1955T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430686 | |||||||
| chr2:27430720 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+1989A>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430720 | |||||||
| chr2:27430740 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-21+2009G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430740 | |||||||
| chr2:27430768 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-21+2037C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430768 | |||||||
| chr2:27430819 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-21+2088C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27430819 | |||||||
| chr2:27431038 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-20-2216C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27431038 | |||||||
| chr2:27431116 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-20-2138C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27431116 | |||||||
| chr2:27431190 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20-2064C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27431190 | |||||||
| chr2:27431846 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0002g0053 |
3 | HG02145.hp1 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-1408G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27431846 | |||||||
| chr2:27431994 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-20-1260G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27431994 | |||||||
| chr2:27432128 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-20-1126C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432128 | |||||||
| chr2:27432168 | A | G | 1 | a0002c0002t0001g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-20-1086A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432168 | |||||||
| chr2:27432208 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0052 others(1): Show |
11 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-1046A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432208 | |||||||
| chr2:27432253 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0057 a0001c0001t0004g0040 others(1): Show |
5 | HG02257.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-1001T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432253 | |||||||
| chr2:27432277 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-20-977C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432277 | |||||||
| chr2:27432481 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-773C>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432481 | |||||||
| chr2:27432580 | T | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(28): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-20-674T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432580 | |||||||
| chr2:27432637 | A | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01175.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-20-617A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432637 | |||||||
| chr2:27432690 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-20-564A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432690 | |||||||
| chr2:27432701 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-20-553G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432701 | |||||||
| chr2:27432939 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0028 others(3): Show |
14 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-315C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27432939 | |||||||
| chr2:27433001 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-20-253T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27433001 | |||||||
| chr2:27433027 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-20-227G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27433027 | |||||||
| chr2:27433169 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-20-85A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27433169 | |||||||
| chr2:27433171 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-83G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27433171 | |||||||
| chr2:27433227 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-20-27C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 1/17 | chr2 | 27433227 | |||||||
| chr2:27433588 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0055 |
8 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-85G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 2/17 | chr2 | 27433588 | |||||||
| chr2:27433955 | G | GA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
158 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.334-33dupA | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 27433955 | ||||||
| chr2:27433978 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.334-11C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 3/17 | chr2 | 27433978 | |||||||
| chr2:27434238 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.435+148G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 4/17 | chr2 | 27434238 | |||||||
| chr2:27434243 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.435+153C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 4/17 | chr2 | 27434243 | |||||||
| chr2:27434300 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.436-171T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 4/17 | chr2 | 27434300 | |||||||
| chr2:27434377 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.436-94G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 4/17 | chr2 | 27434377 | |||||||
| chr2:27434693 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.526-29G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 5/17 | chr2 | 27434693 | |||||||
| chr2:27434814 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(7): Show |
50 | HG00597.hp1 HG01074.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.566+52C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 6/17 | chr2 | 27434814 | |||||||
| chr2:27434852 | G | T | 1 | a0001c0001t0001g0020 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.566+90G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 6/17 | chr2 | 27434852 | |||||||
| chr2:27434939 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.566+177C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 6/17 | chr2 | 27434939 | |||||||
| chr2:27435263 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.661+36C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27435263 | |||||||
| chr2:27435431 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.661+204A>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27435431 | |||||||
| chr2:27435898 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.661+671C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27435898 | |||||||
| chr2:27435916 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG02257.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.661+689T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27435916 | |||||||
| chr2:27436305 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.662-448A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27436305 | |||||||
| chr2:27436624 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.662-129T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 7/17 | chr2 | 27436624 | |||||||
| chr2:27436957 | T | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0051 |
5 | HG00735.hp2 HG00741.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-90T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 8/17 | chr2 | 27436957 | |||||||
| chr2:27437002 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.746-45G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 8/17 | chr2 | 27437002 | |||||||
| chr2:27437125 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0052 others(1): Show |
11 | HG01891.hp2 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.804+20G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 9/17 | chr2 | 27437125 | |||||||
| chr2:27437387 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.903+27C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27437387 | |||||||
| chr2:27437593 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.903+233C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27437593 | |||||||
| chr2:27437870 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0008g0005 others(2): Show |
12 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+510C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27437870 | |||||||
| chr2:27437934 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0028 others(3): Show |
14 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.903+574C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27437934 | |||||||
| chr2:27437959 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01891.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.903+599G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27437959 | |||||||
| chr2:27438153 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.903+793T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438153 | |||||||
| chr2:27438153 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0099 |
3 | HG01109.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.903+793T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438153 | |||||||
| chr2:27438177 | CA | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.903+832delA | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27438177 | ||||||
| chr2:27438247 | AG | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(43): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.903+889delG | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27438247 | ||||||
| chr2:27438291 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.903+931A>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438291 | |||||||
| chr2:27438419 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.903+1059A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438419 | |||||||
| chr2:27438479 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.903+1119A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438479 | |||||||
| chr2:27438561 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
5 | HG00738.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+1201T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438561 | |||||||
| chr2:27438749 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.904-1017C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438749 | |||||||
| chr2:27438869 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.904-897G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438869 | |||||||
| chr2:27438893 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.904-873A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438893 | |||||||
| chr2:27438963 | A | G | 1 | a0001c0001t0001g0009 | 4 | HG06807.hp2 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-803A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438963 | |||||||
| chr2:27438991 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.904-775C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27438991 | |||||||
| chr2:27439167 | A | G | 1 | a0001c0001t0002g0018 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.904-599A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439167 | |||||||
| chr2:27439200 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.904-566G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439200 | |||||||
| chr2:27439213 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.904-553C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439213 | |||||||
| chr2:27439258 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0055 |
9 | HG00738.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.904-508C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439258 | |||||||
| chr2:27439395 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0081 |
5 | HG00099.hp1 HG01109.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.904-371G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439395 | |||||||
| chr2:27439400 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.904-366G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439400 | |||||||
| chr2:27439441 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.904-325C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439441 | |||||||
| chr2:27439484 | C | CA | 25 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(22): Show |
42 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.904-262dupA | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27439484 | ||||||
| chr2:27439484 | CA | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0050 others(5): Show |
13 | HG00741.hp2 HG01081.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-262delA | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27439484 | ||||||
| chr2:27439505 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.904-261T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439505 | |||||||
| chr2:27439611 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.904-155C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439611 | |||||||
| chr2:27439616 | T | TCAGGTGC others(308): Show |
1 | a0001c0001t0001g0070 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.904-136_904-135ins others(315): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27439616 | ||||||
| chr2:27439616 | T | TCAGGTGC others(313): Show |
1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.904-136_904-135ins others(320): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27439616 | ||||||
| chr2:27439616 | T | TCAGGTGC others(314): Show |
1 | a0001c0001t0001g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.904-136_904-135ins others(321): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 27439616 | ||||||
| chr2:27439701 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.904-65C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439701 | |||||||
| chr2:27439719 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0042 |
3 | HG02280.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.904-47T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 10/17 | chr2 | 27439719 | |||||||
| chr2:27439899 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | splice_donor_variant&intron_variant | HIGH | c.1036+1G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439899 | |||||||
| chr2:27439904 | T | G | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | splice_region_variant&intron_variant | LOW | c.1036+6T>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439904 | |||||||
| chr2:27439905 | C | G | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | splice_region_variant&intron_variant | LOW | c.1036+7C>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439905 | |||||||
| chr2:27439906 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | splice_region_variant&intron_variant | LOW | c.1036+8G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439906 | |||||||
| chr2:27439915 | C | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+17C>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439915 | |||||||
| chr2:27439916 | T | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+18T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439916 | |||||||
| chr2:27439918 | T | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+20T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439918 | |||||||
| chr2:27439919 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+21G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439919 | |||||||
| chr2:27439920 | G | T | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+22G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439920 | |||||||
| chr2:27439921 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+23G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439921 | |||||||
| chr2:27439923 | A | T | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+25A>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439923 | |||||||
| chr2:27439925 | T | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+27T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439925 | |||||||
| chr2:27439926 | A | G | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+28A>G | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439926 | |||||||
| chr2:27439927 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+29G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439927 | |||||||
| chr2:27439937 | C | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+39C>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439937 | |||||||
| chr2:27439945 | C | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+47C>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439945 | |||||||
| chr2:27439946 | T | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+48T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439946 | |||||||
| chr2:27439948 | T | A | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+50T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439948 | |||||||
| chr2:27439949 | A | T | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+51A>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439949 | |||||||
| chr2:27439952 | T | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+54T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439952 | |||||||
| chr2:27439960 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+62G>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439960 | |||||||
| chr2:27439962 | A | T | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+64A>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439962 | |||||||
| chr2:27439964 | G | T | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+66G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439964 | |||||||
| chr2:27439966 | T | C | 1 | a0003c0006t0001g0069 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1036+68T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27439966 | |||||||
| chr2:27439995 | C | CT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0029 others(12): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1036+133dupT | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | C | CTT | 13 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0061 others(10): Show |
52 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1036+132_1036+133d others(4): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | C | CTTT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(8): Show |
21 | HG00609.hp1 HG00609.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.1036+131_1036+133d others(5): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | C | CTTTT | 9 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
12 | HG00597.hp2 HG01169.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1036+130_1036+133d others(6): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | C | CTTTTT | 3 | a0001c0001t0001g0017 a0001c0001t0001g0074 a0001c0001t0001g0077 |
5 | HG01928.hp1 HG02735.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1036+129_1036+133d others(7): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1036+124_1036+133d others(12): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0050 |
9 | HG01358.hp2 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1036+123_1036+133d others(13): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0034 a0001c0001t0002g0053 |
3 | HG02145.hp1 NA19009.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1036+120_1036+133d others(16): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(8): Show |
C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
14 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1036+119_1036+133d others(17): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0043 |
3 | HG00639.hp2 HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1036+118_1036+133d others(18): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 others(1): Show |
11 | HG00733.hp2 HG01167.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036+117_1036+133d others(19): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0018 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1036+116_1036+133d others(20): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0086 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1036+115_1036+133d others(21): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0030 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1036+114_1036+133d others(22): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(14): Show |
C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(27): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1036+113_1036+133d others(23): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27439995 | CTTTTTTT others(15): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1036+112_1036+133d others(24): Show |
NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr2 | 27439995 | ||||||
| chr2:27440255 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1037-148C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27440255 | |||||||
| chr2:27440256 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1037-147G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27440256 | |||||||
| chr2:27440260 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1037-143C>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27440260 | |||||||
| chr2:27440348 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1037-55T>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 11/17 | chr2 | 27440348 | |||||||
| chr2:27440549 | G | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(46): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1142+41G>T | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 12/17 | chr2 | 27440549 | |||||||
| chr2:27441021 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0020 |
6 | HG02559.hp1 HG03453.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329+81T>C | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 14/17 | chr2 | 27441021 | |||||||
| chr2:27441533 | G | A | 1 | a0001c0001t0004g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1448-34G>A | NRBP1 | ENSG00000115216.14 | transcript | ENST00000379852.8 | protein_coding | 16/17 | chr2 | 27441533 |