Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56953 |
| ensemblid | ENSG00000205309.14 |
| hgncid | 15769 |
| symbol | NT5M |
| name | 5',3'-nucleotidase, mitochondrial |
| refseq_nuc | NM_020201.4 |
| refseq_prot | NP_064586.1 |
| ensembl_nuc | ENST00000389022.9 |
| ensembl_prot | ENSP00000373674.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 17303373 |
| end | 17347663 |
| strand | + |
| ver | v1.2 |
| region | chr17:17303373-17347663 |
| region5000 | chr17:17298373-17352663 |
| regionname0 | NT5M_chr17_17303373_17347663 |
| regionname5000 | NT5M_chr17_17298373_17352663 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 228 | 345 | 90 | 76 | 123 | 12 | 42 | 80 | NT5M_chr17_17298373_17352663 | NT5M | MIRLG others(223): Show |
chr17 | 17298373 | 17352663 |
| a0002 | 0/0 | 50 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | MIRLG others(45): Show |
chr17 | 17298373 | 17352663 |
| a0003 | 0/0 | 69 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | MIRLG others(64): Show |
chr17 | 17298373 | 17352663 |
| a0004 | 0/0 | 228 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | MIRLG others(223): Show |
chr17 | 17298373 | 17352663 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 684 | 284 | 88 | 68 | 78 | 12 | 36 | NT5M_chr17_17298373_17352663 | NT5M | ATGAT others(679): Show |
chr17 | 17298373 | 17352663 | ||
| a0001c0002 | 0/0 | 684 | 61 | 2 | 8 | 45 | 0 | 6 | NT5M_chr17_17298373_17352663 | NT5M | ATGAT others(679): Show |
chr17 | 17298373 | 17352663 | ||
| a0002c0003 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | ATGAT others(689): Show |
chr17 | 17298373 | 17352663 | ||
| a0003c0005 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | ATGAT others(679): Show |
chr17 | 17298373 | 17352663 | ||
| a0004c0004 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | ATGAT others(679): Show |
chr17 | 17298373 | 17352663 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1581 | 261 | 76 | 62 | 78 | 10 | 33 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0002 | 0/0 | 1581 | 12 | 4 | 3 | 0 | 2 | 3 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0003 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0004 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0005 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0006 | 0/0 | 1581 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0007 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0008 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0001t0009 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0002t0001 | 0/0 | 1581 | 60 | 2 | 8 | 45 | 0 | 5 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0001c0002t0002 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0002c0003t0001 | 0/0 | 1591 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1586): Show |
chr17 | 17298373 | 17352663 |
| a0003c0005t0001 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| a0004c0004t0001 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | GCTCT others(1576): Show |
chr17 | 17298373 | 17352663 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0003c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| a0004c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0131 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | CHS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0249 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0306 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0304 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0312 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03239 | hp2 | a0003 | c0005 | t0001 | g0087 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0313 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04184 | hp1 | a0004 | c0004 | t0001 | g0276 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | BEB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0296 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | USA | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0202 | REF | REF | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0103 | REF | REF | NT5M_chr17_17298373_17352663 | NT5M | chr17 | 17298373 | 17352663 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17303603 | C | CCGCGGGG others(3): Show |
1 | a0002 | 1 | HG02135.hp1 | frameshift_variant | HIGH | c.66_75dupCGGGGCGGCG | p.Gly26fs | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 254/1581 | 76/687 | 26/228 | INFO_REALIGN_3_PRIME | chr17 | 17303603 | ||
| chr17:17303758 | G | T | 1 | a0003 | 1 | HG03239.hp2 | stop_gained | HIGH | c.208G>T | p.Glu70* | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 386/1581 | 208/687 | 70/228 | chr17 | 17303758 | |||
| chr17:17344897 | C | T | 1 | a0004 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.533C>T | p.Pro178Leu | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/5 | 711/1581 | 533/687 | 178/228 | chr17 | 17344897 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17346845 | C | T | 2 | a0001c0002 a0004c0004 |
62 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(59): Show |
synonymous_variant | LOW | c.585C>T | p.Thr195Thr | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 763/1581 | 585/687 | 195/228 | chr17 | 17346845 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17303402 | C | G | 2 | a0001c0001t0002 a0001c0002t0002 |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-149C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/5 | 149 | chr17 | 17303402 | ||||||
| chr17:17347035 | G | T | 1 | a0001c0001t0006 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*88G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 88 | chr17 | 17347035 | ||||||
| chr17:17347172 | G | A | 1 | a0001c0001t0007 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*225G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 225 | chr17 | 17347172 | ||||||
| chr17:17347281 | T | C | 1 | a0001c0001t0003 | 2 | HG02572.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 334 | chr17 | 17347281 | ||||||
| chr17:17347383 | G | T | 1 | a0001c0001t0009 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 436 | chr17 | 17347383 | ||||||
| chr17:17347439 | C | T | 1 | a0001c0001t0005 | 2 | HG02055.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*492C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 492 | chr17 | 17347439 | ||||||
| chr17:17347581 | G | T | 1 | a0001c0001t0004 | 2 | HG03139.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*634G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 634 | chr17 | 17347581 | ||||||
| chr17:17347603 | C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 5/5 | 656 | chr17 | 17347603 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17303887 | C | G | 33 | a0001c0001t0001g0017 a0001c0001t0001g0295 a0001c0001t0001g0297 others(30): Show |
34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.267+70C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17303887 | |||||||
| chr17:17303908 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.267+91G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17303908 | |||||||
| chr17:17304108 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.267+291C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304108 | |||||||
| chr17:17304210 | GGT | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0297 a0001c0001t0001g0298 others(7): Show |
11 | HG01192.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.267+396_267+397del others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17304210 | ||||||
| chr17:17304296 | TG | T | 35 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.267+484delG | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17304296 | ||||||
| chr17:17304419 | T | C | 1 | a0002c0003t0001g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.267+602T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304419 | |||||||
| chr17:17304500 | G | T | 1 | a0001c0002t0001g0294 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+683G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304500 | |||||||
| chr17:17304501 | C | G | 1 | a0001c0002t0001g0294 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+684C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304501 | |||||||
| chr17:17304502 | A | C | 1 | a0001c0002t0001g0294 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+685A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304502 | |||||||
| chr17:17304595 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.267+778G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304595 | |||||||
| chr17:17304906 | A | G | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.267+1089A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304906 | |||||||
| chr17:17304908 | A | G | 1 | a0001c0002t0001g0259 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.267+1091A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304908 | |||||||
| chr17:17304918 | G | A | 33 | a0001c0001t0001g0017 a0001c0001t0001g0295 a0001c0001t0001g0297 others(30): Show |
34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.267+1101G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304918 | |||||||
| chr17:17304991 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
6 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+1174C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17304991 | |||||||
| chr17:17305103 | G | GGGGAGTC others(24): Show |
1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.267+1294_267+1295i others(33): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305103 | ||||||
| chr17:17305389 | C | T | 33 | a0001c0001t0001g0017 a0001c0001t0001g0295 a0001c0001t0001g0297 others(30): Show |
34 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.268-1154C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305389 | |||||||
| chr17:17305394 | G | GC | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(60): Show |
68 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.268-1136dupC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | ||||||
| chr17:17305394 | G | GCC | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG01099.hp1 HG01175.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.268-1137_268-1136d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | ||||||
| chr17:17305394 | GC | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0109 a0001c0001t0001g0110 others(44): Show |
48 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.268-1136delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | ||||||
| chr17:17305394 | GCC | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(100): Show |
115 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.268-1137_268-1136d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | ||||||
| chr17:17305394 | GCCC | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0231 a0001c0001t0001g0232 others(10): Show |
14 | HG00735.hp2 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.268-1138_268-1136d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305394 | ||||||
| chr17:17305397 | C | G | 16 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0242 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-1146C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305397 | |||||||
| chr17:17305401 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.268-1142C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305401 | |||||||
| chr17:17305401 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.268-1142C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305401 | |||||||
| chr17:17305404 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.268-1139C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305404 | |||||||
| chr17:17305413 | C | T | 35 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.268-1130C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305413 | |||||||
| chr17:17305603 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.268-940C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305603 | |||||||
| chr17:17305603 | CGGCCGTC others(13): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.268-936_268-917del others(20): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr17 | 17305603 | ||||||
| chr17:17305607 | C | T | 18 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0239 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.268-936C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305607 | |||||||
| chr17:17305651 | G | A | 29 | a0001c0001t0001g0017 a0001c0001t0001g0295 a0001c0001t0001g0297 others(26): Show |
30 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.268-892G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305651 | |||||||
| chr17:17305676 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.268-867C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17305676 | |||||||
| chr17:17306339 | C | T | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-204C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306339 | |||||||
| chr17:17306354 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.268-189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306354 | |||||||
| chr17:17306371 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268-172C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306371 | |||||||
| chr17:17306410 | G | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0295 others(17): Show |
21 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.268-133G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306410 | |||||||
| chr17:17306446 | A | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0295 others(17): Show |
21 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.268-97A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 1/4 | chr17 | 17306446 | |||||||
| chr17:17306674 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.368+31T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306674 | |||||||
| chr17:17306732 | T | C | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+89T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306732 | |||||||
| chr17:17306758 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0295 a0001c0001t0001g0321 |
3 | HG00741.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+115G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306758 | |||||||
| chr17:17306792 | G | A | 21 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0109 others(18): Show |
22 | HG00741.hp1 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.368+149G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306792 | |||||||
| chr17:17306919 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.368+276C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306919 | |||||||
| chr17:17306927 | G | C | 1 | a0001c0002t0001g0021 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.368+284G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306927 | |||||||
| chr17:17306945 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.368+302C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306945 | |||||||
| chr17:17306949 | G | C | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+306G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306949 | |||||||
| chr17:17306950 | C | G | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+307C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306950 | |||||||
| chr17:17306972 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
6 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.368+329C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17306972 | |||||||
| chr17:17307040 | A | T | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+397A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307040 | |||||||
| chr17:17307041 | T | A | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+398T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307041 | |||||||
| chr17:17307054 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(212): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.368+411C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307054 | |||||||
| chr17:17307146 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.368+503C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307146 | |||||||
| chr17:17307162 | C | T | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+519C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307162 | |||||||
| chr17:17307269 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.368+626A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307269 | |||||||
| chr17:17307345 | C | T | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368+702C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307345 | |||||||
| chr17:17307346 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.368+703G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307346 | |||||||
| chr17:17307389 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
182 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.368+746C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307389 | |||||||
| chr17:17307394 | C | T | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+751C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307394 | |||||||
| chr17:17307395 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(217): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+752A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307395 | |||||||
| chr17:17307433 | G | C | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+790G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307433 | |||||||
| chr17:17307435 | C | G | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+792C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307435 | |||||||
| chr17:17307466 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.368+823G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307466 | |||||||
| chr17:17307467 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.368+824C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307467 | |||||||
| chr17:17307473 | CTCACGCC others(109): Show |
C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(215): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.368+883_368+998del | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17307473 | ||||||
| chr17:17307478 | GCCTGTAA others(110): Show |
G | 1 | a0001c0002t0001g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.368+837_368+953del | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17307478 | ||||||
| chr17:17307535 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368+892T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307535 | |||||||
| chr17:17307700 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+1057T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307700 | |||||||
| chr17:17307717 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+1074G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307717 | |||||||
| chr17:17307760 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.368+1117G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307760 | |||||||
| chr17:17307776 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.368+1133A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307776 | |||||||
| chr17:17307796 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.368+1153C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307796 | |||||||
| chr17:17307815 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+1172G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307815 | |||||||
| chr17:17307817 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+1174C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307817 | |||||||
| chr17:17307823 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.368+1180A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307823 | |||||||
| chr17:17307860 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.368+1217A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307860 | |||||||
| chr17:17307883 | T | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(37): Show |
41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.368+1240T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307883 | |||||||
| chr17:17307916 | G | C | 1 | a0001c0001t0001g0297 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+1273G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307916 | |||||||
| chr17:17307927 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+1284G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17307927 | |||||||
| chr17:17308024 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+1381T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308024 | |||||||
| chr17:17308042 | CTCTG | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(23): Show |
27 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.368+1403_368+1406d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17308042 | ||||||
| chr17:17308115 | A | G | 27 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(24): Show |
28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.368+1472A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308115 | |||||||
| chr17:17308257 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG02258.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.368+1614G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308257 | |||||||
| chr17:17308329 | C | T | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.368+1686C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308329 | |||||||
| chr17:17308336 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0003g0114 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.368+1693A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308336 | |||||||
| chr17:17308459 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.368+1816G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308459 | |||||||
| chr17:17308524 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.368+1881G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308524 | |||||||
| chr17:17308544 | A | G | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+1901A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308544 | |||||||
| chr17:17308885 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.368+2242G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17308885 | |||||||
| chr17:17309110 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.368+2467A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309110 | |||||||
| chr17:17309113 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.368+2470C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309113 | |||||||
| chr17:17309127 | C | CT | 45 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0148 others(42): Show |
46 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.368+2498dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309127 | ||||||
| chr17:17309127 | C | CTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0269 a0001c0001t0001g0283 others(3): Show |
7 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+2497_368+2498d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309127 | ||||||
| chr17:17309170 | G | A | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+2527G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309170 | |||||||
| chr17:17309448 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+2805G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309448 | |||||||
| chr17:17309465 | G | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+2822G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309465 | |||||||
| chr17:17309513 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+2870A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309513 | |||||||
| chr17:17309675 | C | CTT | 27 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(24): Show |
28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.368+3051_368+3052d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | ||||||
| chr17:17309675 | CT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(92): Show |
100 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.368+3052delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | ||||||
| chr17:17309675 | CTT | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
195 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.368+3051_368+3052d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | ||||||
| chr17:17309675 | CTTT | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0151 a0001c0001t0001g0240 others(3): Show |
6 | HG01070.hp2 HG01257.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+3050_368+3052d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309675 | ||||||
| chr17:17309825 | G | GT | 34 | a0001c0001t0001g0020 a0001c0001t0001g0108 a0001c0001t0001g0138 others(31): Show |
34 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.368+3187dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309825 | ||||||
| chr17:17309831 | G | GT | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(6): Show |
9 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.368+3199dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17309831 | ||||||
| chr17:17309831 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+3188G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309831 | |||||||
| chr17:17309885 | C | T | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3242C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309885 | |||||||
| chr17:17309886 | A | G | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3243A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309886 | |||||||
| chr17:17309887 | C | G | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3244C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309887 | |||||||
| chr17:17309893 | T | C | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368+3250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309893 | |||||||
| chr17:17309903 | C | T | 5 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0005g0018 others(2): Show |
5 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+3260C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17309903 | |||||||
| chr17:17310014 | C | A | 3 | a0001c0001t0001g0116 a0001c0001t0003g0114 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.368+3371C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310014 | |||||||
| chr17:17310158 | T | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+3515T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310158 | |||||||
| chr17:17310194 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+3551A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310194 | |||||||
| chr17:17310284 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.368+3641C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310284 | |||||||
| chr17:17310473 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.368+3830T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310473 | |||||||
| chr17:17310590 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368+3947A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310590 | |||||||
| chr17:17310600 | C | T | 2 | a0001c0001t0002g0309 a0001c0001t0002g0318 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.368+3957C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310600 | |||||||
| chr17:17310663 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.368+4020C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310663 | |||||||
| chr17:17310739 | G | C | 1 | a0001c0002t0001g0153 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.368+4096G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310739 | |||||||
| chr17:17310765 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0154 |
4 | NA18959.hp1 NA18983.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+4122G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17310765 | |||||||
| chr17:17311006 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+4363A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311006 | |||||||
| chr17:17311006 | A | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0101 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.368+4363A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311006 | |||||||
| chr17:17311035 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.368+4392C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311035 | |||||||
| chr17:17311064 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0005g0018 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.368+4421C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311064 | |||||||
| chr17:17311065 | G | A | 13 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(10): Show |
13 | HG01433.hp2 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.368+4422G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311065 | |||||||
| chr17:17311075 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.368+4432G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311075 | |||||||
| chr17:17311103 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.368+4460G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311103 | |||||||
| chr17:17311146 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.368+4503C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311146 | |||||||
| chr17:17311152 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.368+4509C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311152 | |||||||
| chr17:17311210 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0144 others(3): Show |
6 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+4567C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311210 | |||||||
| chr17:17311254 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0252 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.368+4611C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311254 | |||||||
| chr17:17311329 | ACT | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0001g0295 others(3): Show |
6 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+4689_368+4690d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311329 | ||||||
| chr17:17311338 | C | CA | 188 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.368+4708dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311338 | ||||||
| chr17:17311338 | C | CAA | 7 | a0001c0001t0001g0015 a0001c0001t0001g0155 a0001c0001t0001g0219 others(4): Show |
8 | HG01978.hp2 HG02300.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.368+4707_368+4708d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17311338 | ||||||
| chr17:17311461 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368+4818T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311461 | |||||||
| chr17:17311547 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0298 |
2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.368+4904A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311547 | |||||||
| chr17:17311806 | G | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
16 | HG00609.hp2 HG01074.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.368+5163G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311806 | |||||||
| chr17:17311855 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.368+5212G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311855 | |||||||
| chr17:17311920 | G | A | 9 | a0001c0001t0001g0159 a0001c0001t0001g0219 a0001c0002t0001g0009 others(6): Show |
10 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.368+5277G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17311920 | |||||||
| chr17:17312082 | T | C | 40 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(37): Show |
41 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.368+5439T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312082 | |||||||
| chr17:17312268 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(217): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.368+5625A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312268 | |||||||
| chr17:17312360 | G | A | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+5717G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312360 | |||||||
| chr17:17312370 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0293 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.368+5727G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312370 | |||||||
| chr17:17312574 | G | A | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+5931G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312574 | |||||||
| chr17:17312585 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.368+5942G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312585 | |||||||
| chr17:17312601 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(176): Show |
194 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.368+5958G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312601 | |||||||
| chr17:17312644 | C | CA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(211): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.368+6019dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17312644 | ||||||
| chr17:17312644 | C | CAA | 7 | a0001c0001t0001g0160 a0001c0001t0001g0242 a0001c0001t0001g0252 others(4): Show |
7 | HG00423.hp2 HG00438.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.368+6018_368+6019d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17312644 | ||||||
| chr17:17312736 | A | G | 3 | a0001c0001t0001g0212 a0001c0002t0001g0143 a0001c0002t0001g0211 |
3 | HG00735.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.368+6093A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312736 | |||||||
| chr17:17312897 | C | T | 1 | a0002c0003t0001g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.368+6254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312897 | |||||||
| chr17:17312938 | C | T | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+6295C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17312938 | |||||||
| chr17:17313008 | A | G | 54 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0149 others(51): Show |
56 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.368+6365A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313008 | |||||||
| chr17:17313045 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0001g0295 others(3): Show |
6 | HG00741.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+6402G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313045 | |||||||
| chr17:17313101 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.368+6458C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313101 | |||||||
| chr17:17313300 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.368+6657A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313300 | |||||||
| chr17:17313317 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0080 a0001c0001t0001g0148 others(7): Show |
11 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.368+6674T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313317 | |||||||
| chr17:17313484 | C | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0080 others(8): Show |
12 | HG00741.hp1 HG01192.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.368+6841C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313484 | |||||||
| chr17:17313511 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0112 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.368+6868A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313511 | |||||||
| chr17:17313621 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
15 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.368+6978C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313621 | |||||||
| chr17:17313693 | GACATTGG others(1): Show |
G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0036 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.368+7055_368+7062d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17313693 | ||||||
| chr17:17313765 | C | T | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368+7122C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313765 | |||||||
| chr17:17313766 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368+7123G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313766 | |||||||
| chr17:17313773 | C | G | 20 | a0001c0001t0001g0016 a0001c0001t0001g0109 a0001c0001t0001g0261 others(17): Show |
21 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.368+7130C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313773 | |||||||
| chr17:17313774 | A | G | 19 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0148 others(16): Show |
20 | HG00741.hp1 HG01192.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.368+7131A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313774 | |||||||
| chr17:17313787 | G | C | 1 | a0001c0001t0001g0297 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+7144G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313787 | |||||||
| chr17:17313846 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.368+7203A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313846 | |||||||
| chr17:17313873 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.368+7230A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313873 | |||||||
| chr17:17313911 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.368+7268C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313911 | |||||||
| chr17:17313933 | G | A | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.368+7290G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17313933 | |||||||
| chr17:17314010 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.368+7367T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314010 | |||||||
| chr17:17314040 | C | CTTTTTTT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0300 others(2): Show |
6 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+7402_368+7408d others(9): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | ||||||
| chr17:17314040 | C | CTTTTTTT others(1): Show |
17 | a0001c0001t0001g0016 a0001c0001t0001g0148 a0001c0001t0001g0261 others(14): Show |
18 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.368+7401_368+7408d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | ||||||
| chr17:17314040 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0080 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
9 | HG01433.hp2 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.368+7400_368+7408d others(11): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17314040 | ||||||
| chr17:17314194 | C | T | 6 | a0001c0001t0001g0297 a0001c0001t0001g0303 a0001c0001t0001g0323 others(3): Show |
6 | HG02055.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.368+7551C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314194 | |||||||
| chr17:17314392 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.368+7749G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314392 | |||||||
| chr17:17314425 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.368+7782A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314425 | |||||||
| chr17:17314527 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0154 |
4 | NA18959.hp1 NA18983.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.368+7884A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314527 | |||||||
| chr17:17314671 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.368+8028C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314671 | |||||||
| chr17:17314705 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.368+8062C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314705 | |||||||
| chr17:17314740 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.368+8097C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314740 | |||||||
| chr17:17314815 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+8172A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314815 | |||||||
| chr17:17314892 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.368+8249G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314892 | |||||||
| chr17:17314916 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369-8269G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17314916 | |||||||
| chr17:17315069 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.369-8116A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315069 | |||||||
| chr17:17315138 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369-8047A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315138 | |||||||
| chr17:17315138 | AT | A | 33 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0036 others(30): Show |
35 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.369-8038delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315138 | ||||||
| chr17:17315139 | T | A | 1 | a0001c0001t0001g0181 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.369-8046T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315139 | |||||||
| chr17:17315140 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369-8045T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315140 | |||||||
| chr17:17315152 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(134): Show |
147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.369-8033A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315152 | |||||||
| chr17:17315378 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.369-7807A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315378 | |||||||
| chr17:17315545 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
65 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.369-7640T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315545 | |||||||
| chr17:17315568 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.369-7617G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315568 | |||||||
| chr17:17315611 | G | A | 37 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(34): Show |
39 | HG00280.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.369-7574G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315611 | |||||||
| chr17:17315722 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00140.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.369-7463G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315722 | |||||||
| chr17:17315739 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369-7446T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315739 | |||||||
| chr17:17315743 | GGTTTTTT others(1): Show |
G | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.369-7433_369-7426d others(10): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315743 | ||||||
| chr17:17315743 | GGTTTTTT others(5): Show |
G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(35): Show |
40 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.369-7441_369-7430d others(14): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315743 | |||||||
| chr17:17315744 | G | GT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(95): Show |
102 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.369-7434dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | ||||||
| chr17:17315744 | G | GTT | 29 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0075 others(26): Show |
29 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.369-7435_369-7434d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | ||||||
| chr17:17315744 | G | GTTT | 6 | a0001c0001t0001g0242 a0001c0001t0001g0248 a0001c0001t0001g0250 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.369-7436_369-7434d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315744 | ||||||
| chr17:17315744 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.369-7441G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315744 | |||||||
| chr17:17315750 | TTG | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
9 | HG02630.hp2 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-7433_369-7432d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17315750 | ||||||
| chr17:17315751 | TG | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0051 others(14): Show |
18 | HG01070.hp1 HG01109.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.369-7433delG | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315751 | |||||||
| chr17:17315752 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
257 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.369-7433G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315752 | |||||||
| chr17:17315778 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
144 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.369-7407A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315778 | |||||||
| chr17:17315820 | T | G | 51 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(48): Show |
53 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.369-7365T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315820 | |||||||
| chr17:17315840 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0099 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.369-7345C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315840 | |||||||
| chr17:17315912 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0239 others(18): Show |
22 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.369-7273C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315912 | |||||||
| chr17:17315917 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.369-7268A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315917 | |||||||
| chr17:17315945 | T | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0255 a0001c0001t0001g0256 others(6): Show |
10 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-7240T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315945 | |||||||
| chr17:17315948 | C | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0255 a0001c0001t0001g0256 others(6): Show |
10 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-7237C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17315948 | |||||||
| chr17:17316025 | GATTACAG others(296): Show |
G | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-7153_369-6851d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316025 | ||||||
| chr17:17316035 | A | G | 9 | a0001c0001t0001g0138 a0001c0001t0001g0231 a0001c0001t0001g0232 others(6): Show |
9 | HG02258.hp2 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.369-7150A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316035 | |||||||
| chr17:17316045 | A | G | 1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.369-7140A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316045 | |||||||
| chr17:17316051 | G | A | 2 | a0001c0002t0001g0143 a0001c0002t0001g0211 |
2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.369-7134G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316051 | |||||||
| chr17:17316069 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-7116A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316069 | |||||||
| chr17:17316092 | TC | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(62): Show |
70 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.369-7088delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316092 | ||||||
| chr17:17316289 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0080 others(22): Show |
28 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.369-6896C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316289 | |||||||
| chr17:17316304 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-6881C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316304 | |||||||
| chr17:17316345 | A | T | 1 | a0001c0002t0001g0078 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.369-6840A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316345 | |||||||
| chr17:17316369 | T | TTTTA | 187 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.369-6797_369-6794d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316369 | ||||||
| chr17:17316393 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6792G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316393 | |||||||
| chr17:17316621 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.369-6564T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316621 | |||||||
| chr17:17316645 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0275 a0001c0001t0001g0281 |
3 | HG00733.hp2 HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.369-6540G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316645 | |||||||
| chr17:17316693 | TTTTTG | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.369-6467_369-6463d others(7): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316693 | ||||||
| chr17:17316714 | TTTTG | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6467_369-6464d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17316714 | ||||||
| chr17:17316723 | T | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6462T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316723 | |||||||
| chr17:17316724 | G | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6461G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316724 | |||||||
| chr17:17316856 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-6329A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316856 | |||||||
| chr17:17316960 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6225C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17316960 | |||||||
| chr17:17317029 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6156T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317029 | |||||||
| chr17:17317049 | G | GT | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.369-6131dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317049 | ||||||
| chr17:17317055 | G | GT | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.369-6118dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317055 | ||||||
| chr17:17317055 | G | T | 7 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01433.hp2 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.369-6130G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317055 | |||||||
| chr17:17317060 | T | TGTTTTTG | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-6125_369-6124i others(9): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317060 | |||||||
| chr17:17317090 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6095C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317090 | |||||||
| chr17:17317091 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.369-6094C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317091 | |||||||
| chr17:17317107 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-6078T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317107 | |||||||
| chr17:17317135 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-6050T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317135 | |||||||
| chr17:17317250 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-5935C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317250 | |||||||
| chr17:17317284 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-5901G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317284 | |||||||
| chr17:17317398 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.369-5787T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317398 | |||||||
| chr17:17317458 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-5727G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317458 | |||||||
| chr17:17317496 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.369-5689G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317496 | |||||||
| chr17:17317568 | G | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00673.hp2 HG02071.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.369-5617G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317568 | |||||||
| chr17:17317618 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.369-5567T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317618 | |||||||
| chr17:17317687 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.369-5498G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317687 | |||||||
| chr17:17317691 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-5494A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317691 | |||||||
| chr17:17317790 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(207): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.369-5395T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317790 | |||||||
| chr17:17317926 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-5259G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317926 | |||||||
| chr17:17317931 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0255 others(8): Show |
12 | HG01934.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.369-5254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317931 | |||||||
| chr17:17317962 | C | CA | 24 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0052 others(21): Show |
24 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.369-5202dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | ||||||
| chr17:17317962 | C | CAA | 172 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(169): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.369-5203_369-5202d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | ||||||
| chr17:17317962 | C | CAAA | 11 | a0001c0001t0001g0022 a0001c0001t0001g0031 a0001c0001t0001g0062 others(8): Show |
11 | HG00438.hp1 HG00438.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.369-5204_369-5202d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17317962 | ||||||
| chr17:17317996 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.369-5189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17317996 | |||||||
| chr17:17318000 | CTGTA | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-5182_369-5179d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318000 | ||||||
| chr17:17318345 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.369-4840T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318345 | |||||||
| chr17:17318383 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.369-4802C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318383 | |||||||
| chr17:17318411 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369-4774C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318411 | |||||||
| chr17:17318437 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.369-4748T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318437 | |||||||
| chr17:17318480 | C | CA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
160 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.369-4682dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | ||||||
| chr17:17318480 | C | CAA | 35 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0107 others(32): Show |
35 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.369-4683_369-4682d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | ||||||
| chr17:17318480 | CAAAAAA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(4): Show |
8 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.369-4687_369-4682d others(8): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318480 | ||||||
| chr17:17318645 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.369-4540C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318645 | |||||||
| chr17:17318785 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
159 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.369-4376dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | ||||||
| chr17:17318785 | C | CAA | 14 | a0001c0001t0001g0062 a0001c0001t0001g0138 a0001c0001t0001g0146 others(11): Show |
14 | HG00438.hp1 HG00438.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.369-4377_369-4376d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | ||||||
| chr17:17318785 | CA | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
128 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.369-4376delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | ||||||
| chr17:17318785 | CAA | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0083 a0001c0001t0001g0148 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-4377_369-4376d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17318785 | ||||||
| chr17:17318787 | A | G | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.369-4398A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318787 | |||||||
| chr17:17318857 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.369-4328A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318857 | |||||||
| chr17:17318876 | G | A | 4 | a0001c0001t0002g0305 a0001c0001t0002g0307 a0001c0001t0002g0309 others(1): Show |
4 | HG01891.hp2 HG02258.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-4309G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318876 | |||||||
| chr17:17318926 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.369-4259A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318926 | |||||||
| chr17:17318960 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(68): Show |
77 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.369-4225C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17318960 | |||||||
| chr17:17319105 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369-4080C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319105 | |||||||
| chr17:17319175 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-4010C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319175 | |||||||
| chr17:17319213 | G | GA | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.369-3956dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17319213 | ||||||
| chr17:17319219 | A | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-3966A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319219 | |||||||
| chr17:17319569 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.369-3616G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319569 | |||||||
| chr17:17319732 | GGACAGCT others(6): Show |
G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-3450_369-3438d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17319732 | ||||||
| chr17:17319767 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-3418A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319767 | |||||||
| chr17:17319935 | T | C | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.369-3250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17319935 | |||||||
| chr17:17320018 | T | A | 1 | a0001c0002t0001g0233 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.369-3167T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320018 | |||||||
| chr17:17320097 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0252 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.369-3088C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320097 | |||||||
| chr17:17320124 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-3061G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320124 | |||||||
| chr17:17320144 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.369-3041C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320144 | |||||||
| chr17:17320189 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.369-2996A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320189 | |||||||
| chr17:17320362 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-2823A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320362 | |||||||
| chr17:17320429 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.369-2756A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320429 | |||||||
| chr17:17320537 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.369-2648T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320537 | |||||||
| chr17:17320547 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.369-2638G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320547 | |||||||
| chr17:17320628 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.369-2557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320628 | |||||||
| chr17:17320706 | A | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.369-2479A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320706 | |||||||
| chr17:17320763 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0005g0018 a0001c0001t0005g0033 |
3 | HG02055.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.369-2422C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320763 | |||||||
| chr17:17320850 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.369-2335C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17320850 | |||||||
| chr17:17321025 | CA | C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0051 others(12): Show |
15 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-2159delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321025 | |||||||
| chr17:17321104 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.369-2081G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321104 | |||||||
| chr17:17321217 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1968G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321217 | |||||||
| chr17:17321228 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.369-1957G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321228 | |||||||
| chr17:17321235 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0180 others(4): Show |
7 | HG02027.hp1 NA18970.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.369-1950G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321235 | |||||||
| chr17:17321238 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0032 |
2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.369-1947T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321238 | |||||||
| chr17:17321299 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.369-1886C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321299 | |||||||
| chr17:17321432 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1753A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321432 | |||||||
| chr17:17321485 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.369-1700G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321485 | |||||||
| chr17:17321546 | GGCTGTGC others(11): Show |
G | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1637_369-1620d others(20): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17321546 | ||||||
| chr17:17321671 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-1514A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321671 | |||||||
| chr17:17321721 | T | G | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.369-1464T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321721 | |||||||
| chr17:17321724 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.369-1461G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321724 | |||||||
| chr17:17321781 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369-1404G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321781 | |||||||
| chr17:17321958 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
13 | HG02622.hp1 HG02818.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.369-1227G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17321958 | |||||||
| chr17:17322076 | C | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.369-1109C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322076 | |||||||
| chr17:17322083 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0003g0114 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.369-1102A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322083 | |||||||
| chr17:17322218 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369-967G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322218 | |||||||
| chr17:17322229 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0005g0018 a0001c0001t0005g0033 |
3 | HG02055.hp1 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.369-956G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322229 | |||||||
| chr17:17322347 | G | A | 1 | a0001c0001t0002g0309 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.369-838G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322347 | |||||||
| chr17:17322387 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0015 others(65): Show |
72 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.369-798T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322387 | |||||||
| chr17:17322443 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-742G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322443 | |||||||
| chr17:17322511 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.369-674G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322511 | |||||||
| chr17:17322515 | C | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.369-670C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322515 | |||||||
| chr17:17322596 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
5 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.369-589C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322596 | |||||||
| chr17:17322603 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.369-582C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322603 | |||||||
| chr17:17322689 | G | GAGGGC | 180 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(177): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.369-495_369-491dup others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17322689 | ||||||
| chr17:17322695 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.369-490G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322695 | |||||||
| chr17:17322731 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0111 a0001c0001t0001g0180 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.369-454G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322731 | |||||||
| chr17:17322776 | AGCCAAGC others(4): Show |
A | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.369-400_369-390del others(11): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr17 | 17322776 | ||||||
| chr17:17322808 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0203 others(17): Show |
22 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.369-377A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322808 | |||||||
| chr17:17322953 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369-232G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 2/4 | chr17 | 17322953 | |||||||
| chr17:17323643 | C | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0300 a0001c0001t0001g0301 others(5): Show |
9 | HG01192.hp1 HG01891.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+398C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323643 | |||||||
| chr17:17323671 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0099 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.429+426C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323671 | |||||||
| chr17:17323749 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.429+504C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323749 | |||||||
| chr17:17323758 | A | G | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+513A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323758 | |||||||
| chr17:17323797 | G | C | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+552G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323797 | |||||||
| chr17:17323818 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.429+573C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323818 | |||||||
| chr17:17323867 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.429+622C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17323867 | |||||||
| chr17:17324137 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.429+892C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324137 | |||||||
| chr17:17324150 | T | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0148 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.429+905T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324150 | |||||||
| chr17:17324212 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.429+967G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324212 | |||||||
| chr17:17324354 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0255 others(4): Show |
8 | HG02615.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+1109C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324354 | |||||||
| chr17:17324397 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.429+1152T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324397 | |||||||
| chr17:17324494 | C | G | 4 | a0001c0001t0001g0265 a0001c0001t0001g0269 a0001c0001t0001g0274 others(1): Show |
4 | HG03041.hp2 HG03209.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1249C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324494 | |||||||
| chr17:17324500 | T | TA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.429+1255_429+1256i others(3): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324500 | |||||||
| chr17:17324501 | T | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.429+1256T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324501 | |||||||
| chr17:17324501 | T | TA | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1269dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17324501 | ||||||
| chr17:17324652 | A | G | 24 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0148 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.429+1407A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324652 | |||||||
| chr17:17324674 | A | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(207): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.429+1429A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324674 | |||||||
| chr17:17324757 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.429+1512C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324757 | |||||||
| chr17:17324853 | C | T | 1 | a0001c0001t0001g0002 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.429+1608C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324853 | |||||||
| chr17:17324877 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0321 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.429+1632C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324877 | |||||||
| chr17:17324914 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.429+1669C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324914 | |||||||
| chr17:17324924 | T | G | 1 | a0001c0002t0001g0173 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.429+1679T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324924 | |||||||
| chr17:17324954 | C | T | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02717.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+1709C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324954 | |||||||
| chr17:17324967 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.429+1722C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17324967 | |||||||
| chr17:17325060 | TC | T | 11 | a0001c0001t0001g0035 a0001c0001t0001g0240 a0001c0001t0001g0242 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.429+1816delC | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325060 | |||||||
| chr17:17325114 | A | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0144 a0001c0001t0001g0215 others(2): Show |
5 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+1869A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325114 | |||||||
| chr17:17325141 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.429+1896T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325141 | |||||||
| chr17:17325184 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.429+1939G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325184 | |||||||
| chr17:17325205 | G | C | 1 | a0001c0002t0002g0312 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.429+1960G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325205 | |||||||
| chr17:17325219 | A | G | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(27): Show |
32 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.429+1974A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325219 | |||||||
| chr17:17325243 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0088 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.429+1998C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325243 | |||||||
| chr17:17325289 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.429+2044G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325289 | |||||||
| chr17:17325291 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.429+2046G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325291 | |||||||
| chr17:17325304 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0203 others(16): Show |
21 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.429+2059G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325304 | |||||||
| chr17:17325326 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.429+2081A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325326 | |||||||
| chr17:17325495 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.429+2250T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325495 | |||||||
| chr17:17325640 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
161 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.429+2395C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325640 | |||||||
| chr17:17325649 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.429+2404T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325649 | |||||||
| chr17:17325741 | C | G | 10 | a0001c0001t0001g0031 a0001c0001t0001g0126 a0001c0001t0001g0146 others(7): Show |
10 | HG00673.hp2 HG02056.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.429+2496C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325741 | |||||||
| chr17:17325867 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+2622A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325867 | |||||||
| chr17:17325894 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.429+2649T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325894 | |||||||
| chr17:17325903 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429+2658A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17325903 | |||||||
| chr17:17326059 | C | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0080 others(23): Show |
27 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.429+2814C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326059 | |||||||
| chr17:17326081 | T | C | 2 | a0001c0001t0002g0319 a0001c0001t0002g0320 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.429+2836T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326081 | |||||||
| chr17:17326244 | C | A | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+2999C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326244 | |||||||
| chr17:17326313 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.429+3068C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326313 | |||||||
| chr17:17326314 | G | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3069G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326314 | |||||||
| chr17:17326396 | C | G | 1 | a0001c0001t0002g0309 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.429+3151C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326396 | |||||||
| chr17:17326397 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.429+3152C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326397 | |||||||
| chr17:17326425 | A | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3180A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326425 | |||||||
| chr17:17326478 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0317 |
3 | HG02717.hp2 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.429+3233G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326478 | |||||||
| chr17:17326547 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+3302G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326547 | |||||||
| chr17:17326553 | G | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0080 a0001c0001t0001g0108 others(18): Show |
22 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.429+3308G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326553 | |||||||
| chr17:17326924 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0085 others(3): Show |
6 | HG01074.hp1 HG01496.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+3679G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326924 | |||||||
| chr17:17326980 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01074.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.429+3735C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17326980 | |||||||
| chr17:17327060 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429+3815C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327060 | |||||||
| chr17:17327060 | CGCCACCA others(869): Show |
C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(186): Show |
203 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.429+3823_429+4698d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327060 | ||||||
| chr17:17327202 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0080 others(30): Show |
36 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.429+3957A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327202 | |||||||
| chr17:17327344 | A | AT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0262 others(2): Show |
7 | HG01069.hp2 HG01071.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+4114dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327344 | ||||||
| chr17:17327344 | AT | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG01074.hp1 HG01496.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.429+4114delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17327344 | ||||||
| chr17:17327707 | G | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(16): Show |
19 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+4462G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327707 | |||||||
| chr17:17327737 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0088 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.429+4492C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17327737 | |||||||
| chr17:17328010 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.429+4765G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328010 | |||||||
| chr17:17328117 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(101): Show |
113 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.429+4872G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328117 | |||||||
| chr17:17328121 | G | C | 2 | a0001c0001t0006g0241 a0001c0001t0006g0249 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.429+4876G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328121 | |||||||
| chr17:17328294 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.429+5049G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328294 | |||||||
| chr17:17328385 | G | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0317 |
2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.429+5140G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328385 | |||||||
| chr17:17328385 | GGAGAAGT others(6): Show |
G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+5149_429+5161d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17328385 | ||||||
| chr17:17328566 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(291): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.429+5321G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328566 | |||||||
| chr17:17328569 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.429+5324G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328569 | |||||||
| chr17:17328687 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0199 |
2 | HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.429+5442G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328687 | |||||||
| chr17:17328928 | G | T | 19 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+5683G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17328928 | |||||||
| chr17:17329047 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0148 a0001c0001t0008g0304 |
3 | HG02145.hp2 HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.429+5802G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329047 | |||||||
| chr17:17329103 | G | A | 4 | a0001c0001t0001g0093 a0001c0001t0001g0269 a0001c0001t0001g0274 others(1): Show |
4 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+5858G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329103 | |||||||
| chr17:17329214 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.429+5969G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329214 | |||||||
| chr17:17329226 | C | A | 8 | a0001c0001t0001g0265 a0001c0001t0001g0267 a0001c0001t0001g0272 others(5): Show |
8 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.429+5981C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329226 | |||||||
| chr17:17329240 | G | A | 74 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(71): Show |
75 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.429+5995G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329240 | |||||||
| chr17:17329264 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(10): Show |
13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+6019C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329264 | |||||||
| chr17:17329270 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+6025G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329270 | |||||||
| chr17:17329284 | T | G | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
80 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.429+6039T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329284 | |||||||
| chr17:17329352 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.429+6107A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329352 | |||||||
| chr17:17329364 | G | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0108 a0001c0001t0001g0219 others(5): Show |
9 | HG00140.hp1 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+6119G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329364 | |||||||
| chr17:17329369 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.429+6124G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329369 | |||||||
| chr17:17329412 | C | T | 6 | a0001c0001t0001g0122 a0001c0001t0001g0186 a0001c0001t0001g0270 others(3): Show |
6 | HG02630.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.429+6167C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329412 | |||||||
| chr17:17329619 | A | C | 1 | a0001c0001t0001g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.429+6374A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329619 | |||||||
| chr17:17329653 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.429+6408G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329653 | |||||||
| chr17:17329858 | G | A | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+6613G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329858 | |||||||
| chr17:17329932 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.429+6687A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329932 | |||||||
| chr17:17329938 | T | C | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+6693T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17329938 | |||||||
| chr17:17330023 | G | C | 5 | a0001c0001t0001g0175 a0001c0001t0001g0187 a0001c0001t0001g0190 others(2): Show |
5 | HG01106.hp2 HG02148.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.429+6778G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330023 | |||||||
| chr17:17330088 | C | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
175 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.429+6843C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330088 | |||||||
| chr17:17330128 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.429+6883G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330128 | |||||||
| chr17:17330177 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+6932G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330177 | |||||||
| chr17:17330236 | G | A | 69 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+6991G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330236 | |||||||
| chr17:17330297 | C | CA | 21 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0041 others(18): Show |
22 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.429+7065dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330297 | ||||||
| chr17:17330308 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.429+7063A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330308 | |||||||
| chr17:17330316 | A | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0316 |
2 | HG00741.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.429+7071A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330316 | |||||||
| chr17:17330321 | A | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0163 a0001c0001t0001g0269 others(3): Show |
6 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+7076A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330321 | |||||||
| chr17:17330334 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.429+7089T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330334 | |||||||
| chr17:17330366 | G | C | 6 | a0001c0001t0001g0286 a0001c0001t0001g0288 a0001c0001t0001g0289 others(3): Show |
6 | HG01433.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+7121G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330366 | |||||||
| chr17:17330379 | C | CT | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+7149dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330379 | ||||||
| chr17:17330379 | CT | C | 14 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(11): Show |
14 | HG00609.hp1 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.429+7149delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330379 | ||||||
| chr17:17330432 | A | G | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.429+7187A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330432 | |||||||
| chr17:17330436 | C | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+7191C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330436 | |||||||
| chr17:17330536 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.429+7291C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330536 | |||||||
| chr17:17330630 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0057 a0001c0001t0001g0097 |
3 | HG02922.hp1 HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.429+7385C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330630 | |||||||
| chr17:17330686 | A | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0183 |
3 | HG02027.hp1 NA19064.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.429+7441A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330686 | |||||||
| chr17:17330729 | T | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0024 others(18): Show |
24 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.429+7484T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330729 | |||||||
| chr17:17330742 | C | CT | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.429+7515dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | ||||||
| chr17:17330742 | CT | C | 62 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
65 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.429+7515delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | ||||||
| chr17:17330742 | CTT | C | 19 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0122 others(16): Show |
19 | HG01934.hp1 HG02055.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+7514_429+7515d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17330742 | ||||||
| chr17:17330745 | T | TC | 11 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.429+7500_429+7501i others(3): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330745 | |||||||
| chr17:17330746 | T | C | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.429+7501T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330746 | |||||||
| chr17:17330781 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+7536C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330781 | |||||||
| chr17:17330867 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(166): Show |
182 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.429+7622C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330867 | |||||||
| chr17:17330868 | G | A | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+7623G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330868 | |||||||
| chr17:17330941 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7696T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330941 | |||||||
| chr17:17330943 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7698G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330943 | |||||||
| chr17:17330948 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7703G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330948 | |||||||
| chr17:17330949 | C | G | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7704C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330949 | |||||||
| chr17:17330955 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7710C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330955 | |||||||
| chr17:17330957 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7712A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330957 | |||||||
| chr17:17330965 | A | T | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7720A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330965 | |||||||
| chr17:17330972 | AGCTCAGG others(1048): Show |
A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+7728_429+8782d others(2): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330972 | |||||||
| chr17:17330985 | G | A | 2 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.429+7740G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17330985 | |||||||
| chr17:17331021 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(10): Show |
13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+7776C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331021 | |||||||
| chr17:17331059 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.429+7814A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331059 | |||||||
| chr17:17331141 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.429+7896A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331141 | |||||||
| chr17:17331216 | C | T | 25 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0044 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.429+7971C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331216 | |||||||
| chr17:17331289 | C | CGT | 19 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.429+8047_429+8048d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17331289 | ||||||
| chr17:17331326 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(10): Show |
13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+8081G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331326 | |||||||
| chr17:17331409 | C | T | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0231 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+8164C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331409 | |||||||
| chr17:17331619 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 |
3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+8374A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331619 | |||||||
| chr17:17331811 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.429+8566C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17331811 | |||||||
| chr17:17332027 | G | A | 1 | a0001c0002t0001g0145 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.429+8782G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332027 | |||||||
| chr17:17332048 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8803A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332048 | |||||||
| chr17:17332059 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8814T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332059 | |||||||
| chr17:17332060 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.429+8815G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332060 | |||||||
| chr17:17332084 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.429+8839G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332084 | |||||||
| chr17:17332084 | GTAT | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+8844_429+8846d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17332084 | ||||||
| chr17:17332152 | A | G | 76 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(73): Show |
79 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.429+8907A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332152 | |||||||
| chr17:17332223 | T | C | 80 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.429+8978T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332223 | |||||||
| chr17:17332271 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0090 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.429+9026G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332271 | |||||||
| chr17:17332310 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(10): Show |
13 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.429+9065G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332310 | |||||||
| chr17:17332421 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0255 others(3): Show |
8 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.429+9176C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332421 | |||||||
| chr17:17332445 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.429+9200C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332445 | |||||||
| chr17:17332475 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.429+9230C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332475 | |||||||
| chr17:17332567 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.429+9322C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332567 | |||||||
| chr17:17332733 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 |
3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.429+9488A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332733 | |||||||
| chr17:17332802 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0092 a0001c0001t0001g0185 |
3 | HG00544.hp2 NA19007.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.429+9557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332802 | |||||||
| chr17:17332939 | T | C | 1 | a0002c0003t0001g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.429+9694T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17332939 | |||||||
| chr17:17333119 | T | G | 2 | a0001c0002t0001g0129 a0001c0002t0001g0222 |
2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.429+9874T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333119 | |||||||
| chr17:17333168 | T | C | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.429+9923T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333168 | |||||||
| chr17:17333312 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.429+10067T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333312 | |||||||
| chr17:17333647 | A | G | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0231 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.429+10402A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333647 | |||||||
| chr17:17333834 | A | AT | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0125 others(3): Show |
6 | HG01175.hp1 HG02056.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.429+10606dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17333834 | ||||||
| chr17:17333834 | AT | A | 46 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(43): Show |
47 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.429+10606delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17333834 | ||||||
| chr17:17333854 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.429+10609G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333854 | |||||||
| chr17:17333943 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.429+10698C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17333943 | |||||||
| chr17:17334198 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.430-10596G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334198 | |||||||
| chr17:17334202 | A | G | 8 | a0001c0001t0001g0093 a0001c0001t0001g0231 a0001c0001t0001g0232 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-10592A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334202 | |||||||
| chr17:17334313 | G | GT | 9 | a0001c0001t0001g0107 a0001c0001t0001g0151 a0001c0001t0001g0207 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.430-10467dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334313 | ||||||
| chr17:17334313 | G | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0070 others(4): Show |
7 | HG02040.hp2 HG03831.hp1 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-10481G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334313 | |||||||
| chr17:17334478 | G | GT | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.430-10297dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334478 | ||||||
| chr17:17334478 | GT | G | 11 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0197 others(8): Show |
11 | HG01074.hp1 HG01257.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-10297delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17334478 | ||||||
| chr17:17334518 | C | T | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-10276C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334518 | |||||||
| chr17:17334574 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.430-10220C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334574 | |||||||
| chr17:17334601 | G | C | 32 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(29): Show |
32 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.430-10193G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334601 | |||||||
| chr17:17334644 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0265 a0001c0001t0001g0267 others(6): Show |
11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-10150T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334644 | |||||||
| chr17:17334716 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0084 others(2): Show |
5 | HG02523.hp1 NA18940.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-10078C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334716 | |||||||
| chr17:17334717 | G | T | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-10077G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334717 | |||||||
| chr17:17334744 | G | T | 69 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(66): Show |
72 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.430-10050G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334744 | |||||||
| chr17:17334804 | G | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0044 others(22): Show |
26 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.430-9990G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17334804 | |||||||
| chr17:17335069 | A | G | 19 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.430-9725A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335069 | |||||||
| chr17:17335096 | G | GT | 7 | a0001c0001t0001g0110 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-9687dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335096 | ||||||
| chr17:17335122 | CTT | C | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0231 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-9670_430-9669d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335122 | ||||||
| chr17:17335208 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.430-9586T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335208 | |||||||
| chr17:17335250 | A | G | 70 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
73 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.430-9544A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335250 | |||||||
| chr17:17335392 | G | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0231 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-9402G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335392 | |||||||
| chr17:17335524 | A | G | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-9270A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335524 | |||||||
| chr17:17335602 | C | T | 1 | a0003c0005t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.430-9192C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335602 | |||||||
| chr17:17335663 | T | C | 124 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
127 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.430-9131T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335663 | |||||||
| chr17:17335669 | GTCAC | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0099 |
3 | HG00639.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.430-9121_430-9118d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17335669 | ||||||
| chr17:17335793 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-9001C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335793 | |||||||
| chr17:17335849 | C | G | 6 | a0001c0001t0001g0105 a0001c0001t0001g0257 a0001c0001t0001g0266 others(3): Show |
6 | HG01934.hp1 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-8945C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17335849 | |||||||
| chr17:17336000 | C | CT | 28 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(25): Show |
28 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.430-8774dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | ||||||
| chr17:17336000 | C | CTT | 16 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(13): Show |
16 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.430-8775_430-8774d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | ||||||
| chr17:17336000 | CT | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0090 others(15): Show |
18 | HG01069.hp1 HG01168.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.430-8774delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336000 | ||||||
| chr17:17336237 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-8557C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336237 | |||||||
| chr17:17336284 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0088 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.430-8510G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336284 | |||||||
| chr17:17336366 | C | T | 6 | a0001c0002t0001g0106 a0001c0002t0001g0168 a0001c0002t0001g0169 others(3): Show |
6 | NA18942.hp2 NA18950.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8428C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336366 | |||||||
| chr17:17336539 | A | C | 2 | a0001c0002t0001g0026 a0001c0002t0001g0259 |
2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.430-8255A>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336539 | |||||||
| chr17:17336554 | CT | C | 73 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
76 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.430-8224delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17336554 | ||||||
| chr17:17336573 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 |
3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.430-8221C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336573 | |||||||
| chr17:17336723 | G | A | 6 | a0001c0002t0001g0106 a0001c0002t0001g0168 a0001c0002t0001g0169 others(3): Show |
6 | NA18942.hp2 NA18950.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-8071G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336723 | |||||||
| chr17:17336931 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430-7863A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17336931 | |||||||
| chr17:17337166 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.430-7628T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337166 | |||||||
| chr17:17337404 | AT | A | 42 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0025 others(39): Show |
44 | HG00544.hp2 HG01515.hp1 HG01517.hp2 others(41): Show |
intron_variant | MODIFIER | c.430-7376delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17337404 | ||||||
| chr17:17337429 | G | A | 1 | a0001c0001t0001g0002 | 3 | HG01069.hp2 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.430-7365G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337429 | |||||||
| chr17:17337593 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0002g0322 |
2 | HG01243.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.430-7201C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337593 | |||||||
| chr17:17337620 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0264 |
2 | HG01361.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.430-7174G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337620 | |||||||
| chr17:17337924 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.430-6870C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337924 | |||||||
| chr17:17337925 | G | A | 75 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
78 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-6869G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337925 | |||||||
| chr17:17337987 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(74): Show |
80 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.430-6807G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17337987 | |||||||
| chr17:17338195 | CT | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0288 a0001c0001t0001g0290 others(5): Show |
8 | HG01243.hp2 HG01515.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.430-6584delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338195 | ||||||
| chr17:17338215 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0041 others(8): Show |
12 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-6579C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338215 | |||||||
| chr17:17338395 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.430-6399G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338395 | |||||||
| chr17:17338436 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430-6358G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338436 | |||||||
| chr17:17338492 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.430-6302C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338492 | |||||||
| chr17:17338673 | AAG | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0278 others(4): Show |
7 | HG00140.hp1 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-6120_430-6119d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338673 | |||||||
| chr17:17338674 | A | G | 69 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(66): Show |
72 | HG00280.hp1 HG00544.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.430-6120A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338674 | |||||||
| chr17:17338676 | GGTT | G | 29 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0043 others(26): Show |
30 | HG00280.hp1 HG00733.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.430-6117_430-6115d others(5): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338676 | |||||||
| chr17:17338676 | GGTTT | G | 40 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0025 others(37): Show |
42 | HG00544.hp2 HG01515.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.430-6117_430-6114d others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338676 | |||||||
| chr17:17338677 | G | GT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0035 others(32): Show |
36 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.430-6095dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | ||||||
| chr17:17338677 | G | GTT | 6 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0020 others(3): Show |
6 | HG00280.hp2 HG02056.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.430-6096_430-6095d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | ||||||
| chr17:17338677 | GT | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0032 others(39): Show |
46 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.430-6095delT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | ||||||
| chr17:17338677 | GTT | G | 24 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0034 others(21): Show |
24 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.430-6096_430-6095d others(4): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338677 | ||||||
| chr17:17338678 | T | G | 7 | a0001c0001t0001g0112 a0001c0001t0001g0122 a0001c0001t0001g0278 others(4): Show |
7 | HG00140.hp1 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.430-6116T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338678 | |||||||
| chr17:17338726 | A | AT | 80 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.430-6050dupT | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17338726 | ||||||
| chr17:17338740 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-6054T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338740 | |||||||
| chr17:17338867 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430-5927C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338867 | |||||||
| chr17:17338878 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.430-5916C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338878 | |||||||
| chr17:17338975 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0041 others(8): Show |
12 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-5819C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338975 | |||||||
| chr17:17338987 | G | A | 75 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
78 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.430-5807G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17338987 | |||||||
| chr17:17339002 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-5792C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339002 | |||||||
| chr17:17339032 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG00140.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-5762T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339032 | |||||||
| chr17:17339049 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0297 |
3 | HG02055.hp2 HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.430-5745A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339049 | |||||||
| chr17:17339088 | A | G | 2 | a0001c0001t0006g0241 a0001c0001t0006g0249 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.430-5706A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339088 | |||||||
| chr17:17339348 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.430-5446A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339348 | |||||||
| chr17:17339384 | T | G | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-5410T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339384 | |||||||
| chr17:17339489 | C | T | 74 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(71): Show |
77 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.430-5305C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339489 | |||||||
| chr17:17339501 | G | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0269 a0001c0001t0001g0274 others(2): Show |
5 | HG03041.hp2 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.430-5293G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339501 | |||||||
| chr17:17339607 | T | C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0044 others(14): Show |
18 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.430-5187T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339607 | |||||||
| chr17:17339737 | A | T | 67 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(64): Show |
70 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.430-5057A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339737 | |||||||
| chr17:17339907 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0265 a0001c0001t0001g0267 others(6): Show |
11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-4887A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339907 | |||||||
| chr17:17339919 | G | C | 32 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0032 others(29): Show |
32 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.430-4875G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339919 | |||||||
| chr17:17339984 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0223 |
2 | NA18940.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.430-4810G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17339984 | |||||||
| chr17:17340058 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-4736G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340058 | |||||||
| chr17:17340110 | C | T | 10 | a0001c0002t0001g0013 a0001c0002t0001g0021 a0001c0002t0001g0027 others(7): Show |
11 | HG02015.hp2 HG02056.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.430-4684C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340110 | |||||||
| chr17:17340265 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-4529A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340265 | |||||||
| chr17:17340373 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430-4421T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340373 | |||||||
| chr17:17340468 | T | A | 2 | a0001c0001t0001g0148 a0001c0001t0008g0304 |
2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.430-4326T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340468 | |||||||
| chr17:17340603 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0265 a0001c0001t0001g0267 others(6): Show |
11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-4191T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340603 | |||||||
| chr17:17340653 | A | T | 12 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0231 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-4141A>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340653 | |||||||
| chr17:17340715 | T | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0110 a0001c0001t0001g0204 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.430-4079T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340715 | |||||||
| chr17:17340737 | G | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0033 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.430-4057G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340737 | |||||||
| chr17:17340755 | G | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-4039G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340755 | |||||||
| chr17:17340778 | G | A | 2 | a0001c0002t0001g0143 a0001c0002t0001g0211 |
2 | HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.430-4016G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340778 | |||||||
| chr17:17340791 | C | CTGGGATT others(6): Show |
1 | a0001c0002t0001g0217 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.430-4000_430-3988d others(15): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr17 | 17340791 | ||||||
| chr17:17340855 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0303 a0001c0001t0002g0305 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.430-3939T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17340855 | |||||||
| chr17:17341445 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.430-3349T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341445 | |||||||
| chr17:17341536 | C | A | 1 | a0001c0001t0001g0314 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.430-3258C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341536 | |||||||
| chr17:17341724 | C | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0099 |
3 | HG00639.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.430-3070C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341724 | |||||||
| chr17:17341768 | T | C | 17 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0051 others(14): Show |
17 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.430-3026T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341768 | |||||||
| chr17:17341878 | G | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0148 a0001c0001t0001g0265 others(7): Show |
12 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.430-2916G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341878 | |||||||
| chr17:17341961 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0323 |
3 | HG03098.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.430-2833G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17341961 | |||||||
| chr17:17342061 | G | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0017 others(39): Show |
46 | HG01192.hp1 HG01515.hp1 HG01517.hp2 others(43): Show |
intron_variant | MODIFIER | c.430-2733G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342061 | |||||||
| chr17:17342191 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.430-2603T>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342191 | |||||||
| chr17:17342228 | A | G | 2 | a0001c0001t0005g0018 a0001c0001t0005g0033 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.430-2566A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342228 | |||||||
| chr17:17342308 | C | G | 1 | a0001c0002t0001g0009 | 2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430-2486C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342308 | |||||||
| chr17:17342418 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0265 a0001c0001t0001g0267 others(6): Show |
11 | HG01192.hp1 HG01891.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.430-2376G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342418 | |||||||
| chr17:17342592 | G | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
115 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.430-2202G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342592 | |||||||
| chr17:17342722 | C | T | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.430-2072C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342722 | |||||||
| chr17:17342996 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.430-1798C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17342996 | |||||||
| chr17:17343174 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.430-1620G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343174 | |||||||
| chr17:17343436 | T | G | 1 | a0001c0001t0009g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430-1358T>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343436 | |||||||
| chr17:17343484 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0180 |
2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.430-1310C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343484 | |||||||
| chr17:17343532 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.430-1262G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343532 | |||||||
| chr17:17343536 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0323 |
3 | HG03098.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.430-1258C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343536 | |||||||
| chr17:17343540 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.430-1254C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343540 | |||||||
| chr17:17343548 | G | A | 31 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0028 others(28): Show |
33 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.430-1246G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343548 | |||||||
| chr17:17343608 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430-1186G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343608 | |||||||
| chr17:17343635 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.430-1159C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343635 | |||||||
| chr17:17343751 | G | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0316 |
2 | HG00741.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.430-1043G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343751 | |||||||
| chr17:17343812 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
115 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.430-982C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17343812 | |||||||
| chr17:17344100 | G | C | 14 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0058 others(11): Show |
14 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.430-694G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344100 | |||||||
| chr17:17344145 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-649A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344145 | |||||||
| chr17:17344210 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.430-584G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344210 | |||||||
| chr17:17344302 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0159 a0001c0001t0001g0182 others(1): Show |
5 | HG00280.hp2 HG02273.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-492A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344302 | |||||||
| chr17:17344455 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.430-339C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344455 | |||||||
| chr17:17344470 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.430-324T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344470 | |||||||
| chr17:17344505 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430-289G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344505 | |||||||
| chr17:17344671 | G | A | 39 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0028 others(36): Show |
41 | HG01243.hp2 HG01515.hp1 HG01516.hp1 others(38): Show |
intron_variant | MODIFIER | c.430-123G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 3/4 | chr17 | 17344671 | |||||||
| chr17:17345108 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.544+200G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345108 | |||||||
| chr17:17345255 | G | A | 1 | a0001c0001t0008g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.544+347G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345255 | |||||||
| chr17:17345402 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.544+494T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345402 | |||||||
| chr17:17345484 | G | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0033 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.544+576G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345484 | |||||||
| chr17:17345522 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.544+614A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345522 | |||||||
| chr17:17345574 | T | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0035 others(24): Show |
28 | HG00140.hp1 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.544+666T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345574 | |||||||
| chr17:17345634 | C | CA | 33 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0028 others(30): Show |
35 | HG00673.hp2 HG01167.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.544+743dupA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345634 | ||||||
| chr17:17345634 | CA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.544+743delA | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345634 | ||||||
| chr17:17345654 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544+746C>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345654 | |||||||
| chr17:17345654 | C | CAAAAAA | 8 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0054 others(5): Show |
8 | HG01192.hp2 HG01261.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.544+748_544+753dup others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345654 | ||||||
| chr17:17345654 | C | CACAAAA | 5 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0295 others(2): Show |
5 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+747_544+748ins others(6): Show |
NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr17 | 17345654 | ||||||
| chr17:17345807 | T | C | 2 | a0001c0001t0005g0018 a0001c0001t0005g0033 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.544+899T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345807 | |||||||
| chr17:17345899 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.545-906G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345899 | |||||||
| chr17:17345944 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.545-861C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345944 | |||||||
| chr17:17345951 | G | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.545-854G>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17345951 | |||||||
| chr17:17346259 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.545-546G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346259 | |||||||
| chr17:17346292 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.545-513A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346292 | |||||||
| chr17:17346382 | G | T | 2 | a0001c0001t0002g0310 a0001c0001t0002g0311 |
2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.545-423G>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346382 | |||||||
| chr17:17346384 | G | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0033 |
2 | HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.545-421G>A | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346384 | |||||||
| chr17:17346439 | T | C | 8 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0144 others(5): Show |
8 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.545-366T>C | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346439 | |||||||
| chr17:17346537 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.545-268A>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346537 | |||||||
| chr17:17346550 | C | G | 1 | a0001c0002t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.545-255C>G | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346550 | |||||||
| chr17:17346573 | C | T | 14 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0058 others(11): Show |
14 | HG00639.hp2 HG00642.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.545-232C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346573 | |||||||
| chr17:17346616 | C | T | 4 | a0001c0002t0001g0129 a0001c0002t0001g0132 a0001c0002t0001g0221 others(1): Show |
4 | HG00639.hp1 HG00738.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-189C>T | NT5M | ENSG00000205309.14 | transcript | ENST00000389022.9 | protein_coding | 4/4 | chr17 | 17346616 |