Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10403 |
| ensemblid | ENSG00000080986.13 |
| hgncid | 16909 |
| symbol | NDC80 |
| name | NDC80 kinetochore complex component |
| refseq_nuc | NM_006101.3 |
| refseq_prot | NP_006092.1 |
| ensembl_nuc | ENST00000261597.9 |
| ensembl_prot | ENSP00000261597.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 2571557 |
| end | 2616635 |
| strand | + |
| ver | v1.2 |
| region | chr18:2571557-2616635 |
| region5000 | chr18:2566557-2621635 |
| regionname0 | NDC80_chr18_2571557_2616635 |
| regionname5000 | NDC80_chr18_2566557_2621635 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 642 | 297 | 72 | 47 | 138 | 12 | 27 | 105 | NDC80_chr18_2566557_2621635 | NDC80 | MKRSS others(637): Show |
chr18 | 2566557 | 2621635 |
| a0002 | 0/1 | 642 | 68 | 17 | 10 | 21 | 2 | 17 | 15 | NDC80_chr18_2566557_2621635 | NDC80 | MKRSS others(637): Show |
chr18 | 2566557 | 2621635 |
| a0003 | 0/0 | 642 | 34 | 3 | 11 | 16 | 2 | 2 | 12 | NDC80_chr18_2566557_2621635 | NDC80 | MKRSS others(637): Show |
chr18 | 2566557 | 2621635 |
| a0004 | 0/0 | 642 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | MKRSS others(637): Show |
chr18 | 2566557 | 2621635 |
| a0005 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | MKRSS others(637): Show |
chr18 | 2566557 | 2621635 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1926 | 296 | 71 | 47 | 138 | 12 | 27 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 | ||
| a0001c0005 | 0/0 | 1926 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 | ||
| a0002c0002 | 0/1 | 1926 | 68 | 17 | 10 | 21 | 2 | 17 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 | ||
| a0003c0003 | 0/0 | 1926 | 34 | 3 | 11 | 16 | 2 | 2 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 | ||
| a0004c0004 | 0/0 | 1926 | 2 | 0 | 2 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 | ||
| a0005c0006 | 0/0 | 1926 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | ATGAA others(1921): Show |
chr18 | 2566557 | 2621635 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2126 | 294 | 69 | 47 | 138 | 12 | 27 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0001c0001t0003 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0001c0001t0004 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0001c0005t0001 | 0/0 | 2126 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0002c0002t0001 | 0/1 | 2126 | 66 | 15 | 10 | 21 | 2 | 17 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0002c0002t0002 | 0/0 | 2126 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0003c0003t0001 | 0/0 | 2126 | 34 | 3 | 11 | 16 | 2 | 2 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0004c0004t0001 | 0/0 | 2126 | 2 | 0 | 2 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| a0005c0006t0001 | 0/0 | 2126 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | AAATT others(2121): Show |
chr18 | 2566557 | 2621635 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0348 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0004c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0004c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| a0005c0006t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0328 | EUR | GBR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00597 | hp1 | a0003 | c0003 | t0001 | g0095 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0250 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0147 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0260 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00673 | hp1 | a0005 | c0006 | t0001 | g0353 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0267 | EAS | CHS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0265 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0252 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0100 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0356 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01261 | hp1 | a0004 | c0004 | t0001 | g0148 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0258 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0259 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0256 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0247 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0254 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0249 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02040 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0097 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0360 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0261 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CDX | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | CDX | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0341 | EAS | CDX | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0367 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0262 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0370 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0306 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0329 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0345 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0357 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0366 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0048 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0138 | AFR | GWD | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0358 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0350 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0248 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0359 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0326 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0335 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0342 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0257 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0363 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0349 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0347 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0354 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0339 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0368 | AFR | YRI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0096 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0099 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0094 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0098 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0092 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19059 | hp1 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19059 | hp2 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0369 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0008 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0364 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0344 | EUR | TSI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | TSI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | GIH | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | GIH | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0365 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0251 | AFR | ACB | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | USA | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0255 | AFR | USA | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | LWK | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0348 | REF | REF | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0041 | REF | REF | NDC80_chr18_2566557_2621635 | NDC80 | chr18 | 2566557 | 2621635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:2595444 | G | T | 1 | a0003 | 34 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
missense_variant | MODERATE | c.1044G>T | p.Glu348Asp | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/17 | 1180/2126 | 1044/1929 | 348/642 | chr18 | 2595444 | |||
| chr18:2599080 | G | T | 1 | a0004 | 2 | HG00639.hp2 HG01261.hp1 |
missense_variant | MODERATE | c.1283G>T | p.Gly428Val | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/17 | 1419/2126 | 1283/1929 | 428/642 | chr18 | 2599080 | |||
| chr18:2616458 | G | C | 2 | a0002 a0005 |
68 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
missense_variant | MODERATE | c.1813G>C | p.Ala605Pro | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 17/17 | 1949/2126 | 1813/1929 | 605/642 | chr18 | 2616458 | |||
| chr18:2616501 | T | C | 1 | a0005 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1856T>C | p.Leu619Pro | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 17/17 | 1992/2126 | 1856/1929 | 619/642 | chr18 | 2616501 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:2610783 | G | A | 1 | a0001c0005 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.1713G>A | p.Thr571Thr | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/17 | 1849/2126 | 1713/1929 | 571/642 | chr18 | 2610783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:2571562 | C | T | 1 | a0002c0002t0002 | 2 | HG02559.hp1 HG02970.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-131C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/17 | chr18 | 2571562 | |||||||
| chr18:2571570 | T | C | 1 | a0001c0001t0003 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-123T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/17 | 1416 | chr18 | 2571570 | ||||||
| chr18:2571590 | C | T | 1 | a0001c0001t0004 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/17 | 1396 | chr18 | 2571590 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:2571824 | A | G | 50 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(47): Show |
54 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+141A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2571824 | |||||||
| chr18:2571847 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.-10+164A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2571847 | |||||||
| chr18:2572018 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+335T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572018 | |||||||
| chr18:2572057 | C | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-10+374C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572057 | |||||||
| chr18:2572096 | T | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(23): Show |
28 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-10+413T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572096 | |||||||
| chr18:2572210 | G | C | 1 | a0002c0002t0001g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-10+527G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572210 | |||||||
| chr18:2572326 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-10+643G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572326 | |||||||
| chr18:2572333 | A | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-9-644A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572333 | |||||||
| chr18:2572334 | T | C | 271 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-9-643T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572334 | |||||||
| chr18:2572337 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02257.hp2 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-640T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572337 | |||||||
| chr18:2572412 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(26): Show |
32 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-9-565G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572412 | |||||||
| chr18:2572552 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-9-425A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572552 | |||||||
| chr18:2572577 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9-400A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572577 | |||||||
| chr18:2572688 | G | A | 239 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(236): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-9-289G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572688 | |||||||
| chr18:2572729 | C | T | 1 | a0002c0002t0001g0369 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-248C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572729 | |||||||
| chr18:2572791 | A | G | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.-9-186A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572791 | |||||||
| chr18:2572828 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-9-149A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572828 | |||||||
| chr18:2572913 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0316 a0001c0001t0001g0317 others(6): Show |
10 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-9-64T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 1/16 | chr18 | 2572913 | |||||||
| chr18:2573184 | T | G | 1 | a0002c0002t0001g0325 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.101+98T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573184 | |||||||
| chr18:2573188 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
11 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.101+102G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573188 | |||||||
| chr18:2573288 | C | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(31): Show |
37 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.101+202C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573288 | |||||||
| chr18:2573427 | G | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA19062.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.101+341G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573427 | |||||||
| chr18:2573665 | G | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0069 others(13): Show |
18 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.101+579G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573665 | |||||||
| chr18:2573679 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101+593G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573679 | |||||||
| chr18:2573729 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.101+643A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573729 | |||||||
| chr18:2573941 | T | TA | 52 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.101+867dupA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr18 | 2573941 | ||||||
| chr18:2573992 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.101+906T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573992 | |||||||
| chr18:2573995 | G | A | 12 | a0003c0003t0001g0007 a0003c0003t0001g0008 a0003c0003t0001g0091 others(9): Show |
14 | HG00597.hp1 HG01175.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.101+909G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2573995 | |||||||
| chr18:2574056 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.102-933A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2574056 | |||||||
| chr18:2574145 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.102-844C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2574145 | |||||||
| chr18:2574664 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.102-325G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2574664 | |||||||
| chr18:2574783 | C | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00438.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.102-206C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2574783 | |||||||
| chr18:2574795 | A | G | 26 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(23): Show |
29 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(26): Show |
intron_variant | MODIFIER | c.102-194A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 2/16 | chr18 | 2574795 | |||||||
| chr18:2575131 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.179+65G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575131 | |||||||
| chr18:2575141 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179+75A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575141 | |||||||
| chr18:2575200 | A | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
20 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.179+134A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575200 | |||||||
| chr18:2575273 | C | T | 52 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.179+207C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575273 | |||||||
| chr18:2575482 | C | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.179+416C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575482 | |||||||
| chr18:2575647 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+581G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575647 | |||||||
| chr18:2575660 | C | T | 4 | a0002c0002t0001g0365 a0002c0002t0001g0366 a0002c0002t0001g0367 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+594C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575660 | |||||||
| chr18:2575824 | C | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(234): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.179+758C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575824 | |||||||
| chr18:2575937 | T | C | 2 | a0001c0001t0001g0283 a0002c0002t0001g0326 |
2 | HG02630.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.179+871T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575937 | |||||||
| chr18:2575957 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | NA18955.hp1 NA18964.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+891A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575957 | |||||||
| chr18:2575999 | T | TAG | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0104 others(33): Show |
38 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.179+933_179+934ins others(2): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2575999 | |||||||
| chr18:2576002 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0104 others(33): Show |
38 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.179+936G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576002 | |||||||
| chr18:2576003 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0104 others(33): Show |
38 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.179+937G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576003 | |||||||
| chr18:2576004 | C | CTT | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0104 others(33): Show |
38 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.179+938_179+939ins others(2): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576004 | |||||||
| chr18:2576179 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.179+1113C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576179 | |||||||
| chr18:2576228 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+1162G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576228 | |||||||
| chr18:2576281 | A | T | 1 | a0002c0002t0001g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.179+1215A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576281 | |||||||
| chr18:2576329 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.179+1263A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576329 | |||||||
| chr18:2576378 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.179+1312C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576378 | |||||||
| chr18:2576498 | A | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
20 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-1248A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576498 | |||||||
| chr18:2576564 | G | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(193): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.180-1182G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576564 | |||||||
| chr18:2576611 | G | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0136 others(2): Show |
7 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.180-1135G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2576611 | |||||||
| chr18:2577011 | T | A | 6 | a0003c0003t0001g0091 a0003c0003t0001g0092 a0003c0003t0001g0093 others(3): Show |
6 | HG00597.hp1 NA18953.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-735T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577011 | |||||||
| chr18:2577143 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.180-603T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577143 | |||||||
| chr18:2577213 | C | T | 1 | a0003c0003t0001g0096 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.180-533C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577213 | |||||||
| chr18:2577215 | CT | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.180-514delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr18 | 2577215 | ||||||
| chr18:2577215 | CTT | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0052 others(15): Show |
19 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.180-515_180-514del others(2): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr18 | 2577215 | ||||||
| chr18:2577246 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.180-500G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577246 | |||||||
| chr18:2577450 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
20 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-296C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577450 | |||||||
| chr18:2577489 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.180-257C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577489 | |||||||
| chr18:2577588 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(234): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.180-158A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 3/16 | chr18 | 2577588 | |||||||
| chr18:2578338 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.476+197G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 5/16 | chr18 | 2578338 | |||||||
| chr18:2578434 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.476+293G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 5/16 | chr18 | 2578434 | |||||||
| chr18:2578627 | A | C | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0018 others(92): Show |
102 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.477-300A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 5/16 | chr18 | 2578627 | |||||||
| chr18:2579090 | T | A | 1 | a0001c0001t0001g0052 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.579+61T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579090 | |||||||
| chr18:2579233 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
20 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.579+204T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579233 | |||||||
| chr18:2579305 | C | A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0101 others(66): Show |
73 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.579+276C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579305 | |||||||
| chr18:2579306 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+277G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579306 | |||||||
| chr18:2579472 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.579+443G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579472 | |||||||
| chr18:2579613 | GACGGGGT others(4): Show |
G | 1 | a0002c0002t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.579+585_579+595del others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579613 | |||||||
| chr18:2579624 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.579+595A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579624 | |||||||
| chr18:2579634 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+605C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579634 | |||||||
| chr18:2579671 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.579+642C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579671 | |||||||
| chr18:2579681 | C | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+652C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2579681 | |||||||
| chr18:2579919 | G | GA | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+895dupA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2579919 | ||||||
| chr18:2580055 | ATTTCACC others(1): Show |
A | 237 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(234): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.579+1029_579+1036d others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580055 | ||||||
| chr18:2580076 | A | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG00544.hp2 NA18990.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1047A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580076 | |||||||
| chr18:2580102 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.579+1073C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580102 | |||||||
| chr18:2580147 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1118T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580147 | |||||||
| chr18:2580151 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579+1122C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580151 | |||||||
| chr18:2580173 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
44 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.579+1144A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580173 | |||||||
| chr18:2580236 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.579+1207T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580236 | |||||||
| chr18:2580336 | C | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(32): Show |
38 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.579+1307C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580336 | |||||||
| chr18:2580338 | T | C | 44 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(41): Show |
49 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.579+1309T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580338 | |||||||
| chr18:2580370 | G | A | 11 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0164 others(8): Show |
11 | HG02056.hp1 HG02071.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+1341G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580370 | |||||||
| chr18:2580411 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1382C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580411 | |||||||
| chr18:2580472 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.579+1443T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580472 | |||||||
| chr18:2580650 | A | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+1621A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580650 | |||||||
| chr18:2580731 | A | ATTT | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(20): Show |
28 | HG00639.hp2 HG01070.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+1729_579+1731d others(5): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTT | 14 | a0001c0001t0001g0090 a0001c0001t0001g0137 a0001c0001t0001g0154 others(11): Show |
14 | HG01106.hp1 HG01255.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1728_579+1731d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0105 others(20): Show |
25 | HG00621.hp1 HG00639.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.579+1725_579+1731d others(9): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(1): Show |
31 | a0001c0001t0001g0101 a0001c0001t0001g0119 a0001c0001t0001g0120 others(28): Show |
32 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.579+1724_579+1731d others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(2): Show |
10 | a0001c0001t0001g0132 a0003c0003t0001g0008 a0003c0003t0001g0094 others(7): Show |
11 | HG00140.hp2 HG00597.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+1723_579+1731d others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(3): Show |
22 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0089 others(19): Show |
23 | HG00735.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.579+1722_579+1731d others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(4): Show |
47 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
51 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+1721_579+1731d others(13): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(5): Show |
28 | a0001c0001t0001g0088 a0001c0001t0001g0170 a0001c0001t0001g0171 others(25): Show |
28 | HG00423.hp2 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.579+1720_579+1731d others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0001g0016 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
11 | HG00642.hp1 HG01261.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+1719_579+1731d others(15): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG00280.hp1 HG01928.hp1 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1718_579+1731d others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0234 |
2 | HG01981.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.579+1717_579+1731d others(17): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG00280.hp2 HG02056.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1716_579+1731d others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(10): Show |
6 | a0001c0001t0001g0017 a0001c0001t0001g0172 a0001c0001t0001g0238 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+1715_579+1731d others(19): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(11): Show |
3 | a0001c0001t0001g0163 a0001c0001t0001g0241 a0001c0001t0001g0305 |
3 | HG01123.hp1 HG02083.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.579+1714_579+1731d others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.579+1710_579+1731d others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.579+1708_579+1731d others(26): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | AT | A | 50 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0037 others(47): Show |
54 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.579+1731delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | ATT | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0053 others(19): Show |
24 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.579+1730_579+1731d others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(4): Show |
8 | HG01167.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+1723_579+1731d others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(3): Show |
6 | HG02129.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+1722_579+1731d others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1720_579+1731d others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580731 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+1719_579+1731d others(15): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2580731 | ||||||
| chr18:2580837 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.579+1808G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580837 | |||||||
| chr18:2580865 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+1836C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580865 | |||||||
| chr18:2580889 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+1860C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580889 | |||||||
| chr18:2580902 | G | A | 1 | a0002c0002t0001g0356 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.579+1873G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580902 | |||||||
| chr18:2580961 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1932C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2580961 | |||||||
| chr18:2581030 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.579+2001A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581030 | |||||||
| chr18:2581193 | T | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(33): Show |
39 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.579+2164T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581193 | |||||||
| chr18:2581238 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+2209C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581238 | |||||||
| chr18:2581364 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+2335G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581364 | |||||||
| chr18:2581496 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.579+2467A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581496 | |||||||
| chr18:2581607 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0086 a0001c0001t0001g0202 others(3): Show |
8 | NA18944.hp1 NA18946.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+2578C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581607 | |||||||
| chr18:2581906 | C | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+2877C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2581906 | |||||||
| chr18:2582054 | TTTTG | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.580-3023_580-3020d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2582054 | ||||||
| chr18:2582054 | TTTTGTTT others(1): Show |
T | 89 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(86): Show |
96 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.580-3027_580-3020d others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2582054 | ||||||
| chr18:2582233 | C | T | 1 | a0002c0002t0001g0354 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.580-2880C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582233 | |||||||
| chr18:2582269 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2844G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582269 | |||||||
| chr18:2582473 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG02083.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.580-2640T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582473 | |||||||
| chr18:2582600 | G | A | 2 | a0001c0001t0001g0053 a0002c0002t0001g0329 |
2 | HG02735.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.580-2513G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582600 | |||||||
| chr18:2582746 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.580-2367T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582746 | |||||||
| chr18:2582764 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-2349C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582764 | |||||||
| chr18:2582848 | T | C | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(355): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.580-2265T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2582848 | |||||||
| chr18:2583037 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0174 a0001c0001t0001g0192 others(25): Show |
29 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-2076C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583037 | |||||||
| chr18:2583038 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0174 a0001c0001t0001g0192 others(25): Show |
29 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-2075C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583038 | |||||||
| chr18:2583039 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0174 a0001c0001t0001g0192 others(25): Show |
29 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-2074C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583039 | |||||||
| chr18:2583410 | C | T | 1 | a0001c0005t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580-1703C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583410 | |||||||
| chr18:2583558 | A | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1555A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583558 | |||||||
| chr18:2583563 | G | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.580-1550G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583563 | |||||||
| chr18:2583584 | C | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1529C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583584 | |||||||
| chr18:2583636 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.580-1477G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583636 | |||||||
| chr18:2583693 | G | A | 48 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(45): Show |
52 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.580-1420G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583693 | |||||||
| chr18:2583697 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(110): Show |
129 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.580-1399dupA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2583697 | ||||||
| chr18:2583817 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-1296G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583817 | |||||||
| chr18:2583977 | A | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-1136A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583977 | |||||||
| chr18:2583990 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1123T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2583990 | |||||||
| chr18:2584036 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-1077G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584036 | |||||||
| chr18:2584059 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.580-1054G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584059 | |||||||
| chr18:2584113 | C | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-1000C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584113 | |||||||
| chr18:2584116 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.580-997C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584116 | |||||||
| chr18:2584117 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-996G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584117 | |||||||
| chr18:2584273 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.580-840G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584273 | |||||||
| chr18:2584287 | C | CA | 55 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0106 others(52): Show |
59 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.580-811dupA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2584287 | ||||||
| chr18:2584287 | CA | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0034 others(32): Show |
37 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.580-811delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr18 | 2584287 | ||||||
| chr18:2584303 | T | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-810T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584303 | |||||||
| chr18:2584366 | A | G | 1 | a0005c0006t0001g0353 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.580-747A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584366 | |||||||
| chr18:2584371 | G | C | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.580-742G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584371 | |||||||
| chr18:2584411 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
137 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.580-702T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584411 | |||||||
| chr18:2584481 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-632G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584481 | |||||||
| chr18:2584509 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.580-604A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584509 | |||||||
| chr18:2584810 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.580-303G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584810 | |||||||
| chr18:2584843 | A | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.580-270A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584843 | |||||||
| chr18:2584943 | C | T | 1 | a0003c0003t0001g0098 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.580-170C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2584943 | |||||||
| chr18:2585078 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
137 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.580-35G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 6/16 | chr18 | 2585078 | |||||||
| chr18:2585366 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(63): Show |
78 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.669+164G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585366 | |||||||
| chr18:2585447 | A | C | 1 | a0001c0001t0001g0295 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.669+245A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585447 | |||||||
| chr18:2585530 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0243 |
2 | HG00140.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.669+328G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585530 | |||||||
| chr18:2585668 | A | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.669+466A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585668 | |||||||
| chr18:2585676 | G | GT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 others(3): Show |
6 | HG01243.hp1 HG02257.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+482dupT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr18 | 2585676 | ||||||
| chr18:2585908 | A | G | 3 | a0002c0002t0001g0351 a0002c0002t0001g0352 a0002c0002t0001g0369 |
3 | NA19059.hp2 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.669+706A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585908 | |||||||
| chr18:2585985 | C | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
137 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.669+783C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585985 | |||||||
| chr18:2585999 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | HG02976.hp2 HG03041.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+797C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2585999 | |||||||
| chr18:2586159 | A | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0090 others(26): Show |
31 | HG00639.hp2 HG01255.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.669+957A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586159 | |||||||
| chr18:2586278 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(60): Show |
75 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.669+1076G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586278 | |||||||
| chr18:2586317 | C | T | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
28 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.669+1115C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586317 | |||||||
| chr18:2586321 | G | C | 34 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
37 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.669+1119G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586321 | |||||||
| chr18:2586466 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0031 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.669+1264A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586466 | |||||||
| chr18:2586551 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0307 |
3 | HG02622.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.670-1279G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586551 | |||||||
| chr18:2586729 | CA | C | 357 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(354): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.670-1091delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr18 | 2586729 | ||||||
| chr18:2586903 | T | A | 356 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(353): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.670-927T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586903 | |||||||
| chr18:2586908 | G | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
198 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.670-922G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586908 | |||||||
| chr18:2586919 | T | C | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.670-911T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586919 | |||||||
| chr18:2586985 | G | A | 3 | a0002c0002t0001g0330 a0002c0002t0001g0331 a0002c0002t0001g0332 |
3 | NA18948.hp1 NA18978.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.670-845G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2586985 | |||||||
| chr18:2587049 | A | G | 3 | a0003c0003t0001g0248 a0003c0003t0001g0251 a0003c0003t0001g0252 |
3 | HG01106.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.670-781A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587049 | |||||||
| chr18:2587105 | CA | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.670-724delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587105 | |||||||
| chr18:2587117 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670-713A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587117 | |||||||
| chr18:2587177 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.670-653C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587177 | |||||||
| chr18:2587185 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.670-645G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587185 | |||||||
| chr18:2587269 | T | C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
44 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.670-561T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587269 | |||||||
| chr18:2587418 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.670-412T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587418 | |||||||
| chr18:2587644 | CA | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0202 a0001c0001t0001g0221 others(2): Show |
7 | NA18944.hp1 NA18946.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-185delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587644 | |||||||
| chr18:2587708 | C | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.670-122C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 7/16 | chr18 | 2587708 | |||||||
| chr18:2587980 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.763+57G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2587980 | |||||||
| chr18:2587994 | A | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.763+71A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2587994 | |||||||
| chr18:2588026 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.763+103T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588026 | |||||||
| chr18:2588148 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.763+225G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588148 | |||||||
| chr18:2588199 | A | C | 2 | a0002c0002t0001g0040 a0002c0002t0001g0044 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.763+276A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588199 | |||||||
| chr18:2588291 | G | A | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
28 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.763+368G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588291 | |||||||
| chr18:2588297 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.763+374C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588297 | |||||||
| chr18:2588361 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.763+438T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588361 | |||||||
| chr18:2588459 | C | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(38): Show |
46 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.763+536C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588459 | |||||||
| chr18:2588846 | A | G | 1 | a0002c0002t0001g0350 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.764-358A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588846 | |||||||
| chr18:2588898 | A | G | 1 | a0002c0002t0001g0364 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.764-306A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588898 | |||||||
| chr18:2588936 | T | A | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
28 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.764-268T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2588936 | |||||||
| chr18:2589026 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.764-178C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2589026 | |||||||
| chr18:2589158 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.764-46C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2589158 | |||||||
| chr18:2589163 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.764-41C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 8/16 | chr18 | 2589163 | |||||||
| chr18:2589420 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.870+110C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589420 | |||||||
| chr18:2589483 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.870+173C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589483 | |||||||
| chr18:2589680 | TAGTATAT others(170): Show |
T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.871-334_871-158del | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr18 | 2589680 | ||||||
| chr18:2589696 | G | C | 4 | a0002c0002t0001g0365 a0002c0002t0001g0366 a0002c0002t0001g0367 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-322G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589696 | |||||||
| chr18:2589801 | T | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 |
3 | HG02257.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.871-217T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589801 | |||||||
| chr18:2589829 | GT | G | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(83): Show |
91 | HG00099.hp1 HG00140.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.871-176delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr18 | 2589829 | ||||||
| chr18:2589898 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.871-120T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589898 | |||||||
| chr18:2589930 | A | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.871-88A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 9/16 | chr18 | 2589930 | |||||||
| chr18:2590245 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1015+83C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590245 | |||||||
| chr18:2590302 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1015+140G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590302 | |||||||
| chr18:2590306 | T | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1015+144T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590306 | |||||||
| chr18:2590335 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.1015+173T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590335 | |||||||
| chr18:2590336 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1015+174C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590336 | |||||||
| chr18:2590765 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1015+603A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590765 | |||||||
| chr18:2590809 | C | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
50 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.1015+647C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590809 | |||||||
| chr18:2590865 | A | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
44 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.1015+703A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2590865 | |||||||
| chr18:2590913 | G | GT | 33 | a0001c0001t0001g0101 a0003c0003t0001g0007 a0003c0003t0001g0008 others(30): Show |
35 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1015+759dupT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2590913 | ||||||
| chr18:2591023 | G | GC | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1015+862dupC | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2591023 | ||||||
| chr18:2591048 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(32): Show |
38 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.1015+886G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591048 | |||||||
| chr18:2591109 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1015+947G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591109 | |||||||
| chr18:2591176 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1015+1014G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591176 | |||||||
| chr18:2591216 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1015+1054G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591216 | |||||||
| chr18:2591280 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015+1118C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591280 | |||||||
| chr18:2591344 | A | T | 1 | a0002c0002t0001g0026 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1015+1182A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591344 | |||||||
| chr18:2591541 | G | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0086 others(65): Show |
71 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1015+1379G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2591541 | |||||||
| chr18:2591569 | GT | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(22): Show |
28 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.1015+1417delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2591569 | ||||||
| chr18:2591755 | CT | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(125): Show |
134 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1015+1610delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2591755 | ||||||
| chr18:2592337 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1015+2175A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2592337 | |||||||
| chr18:2592358 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(34): Show |
40 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1015+2209dupT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2592358 | ||||||
| chr18:2592395 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(33): Show |
39 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1015+2233G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2592395 | |||||||
| chr18:2592750 | C | T | 1 | a0002c0002t0001g0363 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1015+2588C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2592750 | |||||||
| chr18:2593013 | G | GGT | 40 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0066 others(37): Show |
40 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1016-2362_1016-236 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0055 others(54): Show |
61 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.1016-2364_1016-236 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGTGT | 42 | a0001c0001t0001g0017 a0001c0001t0001g0053 a0001c0001t0001g0054 others(39): Show |
43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.1016-2366_1016-236 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGTGTG others(1): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(11): Show |
16 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1016-2368_1016-236 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0171 |
2 | HG02523.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1016-2370_1016-236 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGTGTG others(5): Show |
2 | a0001c0001t0001g0209 a0003c0003t0001g0264 |
2 | HG02040.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1016-2372_1016-236 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0276 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1016-2374_1016-236 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGT | G | 37 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(34): Show |
41 | HG00639.hp2 HG01261.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.1016-2362_1016-236 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGTGT | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(23): Show |
30 | HG01070.hp2 HG01106.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1016-2364_1016-236 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGTGTGT | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0284 a0001c0001t0001g0296 |
3 | HG02895.hp2 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1016-2366_1016-236 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1016-2374_1016-236 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGTGTGTG others(9): Show |
G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1016-2376_1016-236 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593013 | GGTGTGTG others(11): Show |
G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016-2378_1016-236 others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593013 | ||||||
| chr18:2593040 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1016-2376G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593040 | |||||||
| chr18:2593041 | TGTGTGTG others(8): Show |
T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1016-2374_1016-236 others(19): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593041 | |||||||
| chr18:2593042 | G | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(12): Show |
17 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1016-2374G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593042 | |||||||
| chr18:2593043 | TGTGTGTG others(6): Show |
T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(12): Show |
17 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1016-2372_1016-236 others(17): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593043 | |||||||
| chr18:2593051 | TGTGTC | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-2364_1016-236 others(9): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593051 | |||||||
| chr18:2593054 | G | C | 3 | a0001c0001t0001g0310 a0001c0001t0001g0313 a0001c0001t0001g0315 |
3 | HG02818.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1016-2362G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593054 | |||||||
| chr18:2593054 | G | GTGTGTC | 5 | a0002c0002t0001g0024 a0002c0002t0001g0328 a0002c0002t0001g0339 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593054 | ||||||
| chr18:2593054 | G | GTGTGTGT others(1): Show |
3 | a0002c0002t0001g0326 a0002c0002t0001g0344 a0002c0002t0001g0359 |
3 | HG03654.hp2 HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593054 | ||||||
| chr18:2593054 | G | GTGTGTGT others(3): Show |
4 | a0002c0002t0001g0024 a0002c0002t0001g0327 a0002c0002t0001g0346 others(1): Show |
4 | HG03942.hp1 NA18994.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593054 | ||||||
| chr18:2593054 | G | GTGTGTGT others(5): Show |
2 | a0002c0002t0001g0025 a0002c0002t0001g0361 |
2 | HG00735.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593054 | ||||||
| chr18:2593054 | G | GTGTGTGT others(7): Show |
1 | a0002c0002t0001g0363 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1016-2361_1016-236 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2593054 | ||||||
| chr18:2593055 | T | TGTC | 7 | a0001c0001t0001g0312 a0001c0001t0001g0314 a0002c0002t0001g0340 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(7): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTC | 7 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0002c0002t0001g0306 others(4): Show |
7 | HG00673.hp1 HG02647.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(9): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTGTC | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(13): Show |
22 | HG00423.hp1 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTGTG others(7): Show |
1 | a0002c0002t0001g0362 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1016-2361_1016-236 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTGTG others(2): Show |
5 | a0002c0002t0001g0027 a0002c0002t0001g0329 a0002c0002t0001g0332 others(2): Show |
5 | HG02735.hp2 NA18948.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(13): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTGTG others(4): Show |
4 | a0001c0001t0001g0022 a0002c0002t0001g0026 a0002c0002t0001g0331 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(15): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | T | TGTGTGTG others(6): Show |
6 | a0002c0002t0001g0330 a0002c0002t0001g0333 a0002c0002t0001g0336 others(3): Show |
6 | HG00544.hp1 HG00609.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016-2361_1016-236 others(17): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593055 | TC | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0313 a0001c0001t0001g0315 |
3 | HG02818.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1016-2360delC | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593055 | |||||||
| chr18:2593056 | C | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0317 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1016-2360C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593056 | |||||||
| chr18:2593056 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(55): Show |
70 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.1016-2360C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593056 | |||||||
| chr18:2593057 | T | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016-2359T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593057 | |||||||
| chr18:2593057 | T | TC | 5 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0317 others(2): Show |
6 | HG02109.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016-2359_1016-235 others(5): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593057 | |||||||
| chr18:2593090 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1016-2326T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593090 | |||||||
| chr18:2593140 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1016-2276T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593140 | |||||||
| chr18:2593663 | G | A | 52 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1016-1753G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593663 | |||||||
| chr18:2593699 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1016-1717G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593699 | |||||||
| chr18:2593821 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1016-1595C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593821 | |||||||
| chr18:2593875 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(32): Show |
38 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.1016-1541T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593875 | |||||||
| chr18:2593924 | C | CCAAGA | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1016-1492_1016-149 others(9): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593924 | |||||||
| chr18:2593925 | G | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1016-1491G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593925 | |||||||
| chr18:2593926 | G | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1016-1490G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593926 | |||||||
| chr18:2593953 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1016-1463C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2593953 | |||||||
| chr18:2594027 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1016-1389C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594027 | |||||||
| chr18:2594118 | C | G | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1016-1298C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594118 | |||||||
| chr18:2594343 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 |
3 | HG02257.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1016-1073C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594343 | |||||||
| chr18:2594417 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1016-999A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594417 | |||||||
| chr18:2594417 | A | T | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1016-999A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594417 | |||||||
| chr18:2594550 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1016-866T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594550 | |||||||
| chr18:2594606 | AAGTC | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1016-806_1016-803d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2594606 | ||||||
| chr18:2594631 | G | A | 2 | a0002c0002t0001g0328 a0002c0002t0001g0349 |
2 | HG00099.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1016-785G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594631 | |||||||
| chr18:2594670 | A | G | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00423.hp2 HG02056.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1016-746A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594670 | |||||||
| chr18:2594689 | A | G | 1 | a0003c0003t0001g0256 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1016-727A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594689 | |||||||
| chr18:2594880 | C | G | 2 | a0003c0003t0001g0258 a0003c0003t0001g0259 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1016-536C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594880 | |||||||
| chr18:2594899 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1016-517A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594899 | |||||||
| chr18:2594910 | T | A | 1 | a0002c0002t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1016-506T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2594910 | |||||||
| chr18:2595229 | T | TTATA | 279 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(276): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1016-177_1016-174d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595229 | ||||||
| chr18:2595229 | T | TTATATA | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 others(1): Show |
4 | HG00423.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016-179_1016-174d others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595229 | ||||||
| chr18:2595229 | T | TTATATAT others(1): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(9): Show |
20 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.1016-181_1016-174d others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595229 | ||||||
| chr18:2595229 | T | TTATATAT others(3): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0033 others(15): Show |
20 | HG00597.hp2 HG01891.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.1016-183_1016-174d others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595229 | ||||||
| chr18:2595229 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0066 |
2 | HG00438.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1016-185_1016-174d others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595229 | ||||||
| chr18:2595276 | CATATATA others(2): Show |
C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(91): Show |
103 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1016-121_1016-113d others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr18 | 2595276 | ||||||
| chr18:2595358 | A | G | 2 | a0002c0002t0001g0040 a0002c0002t0001g0044 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1016-58A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 10/16 | chr18 | 2595358 | |||||||
| chr18:2595630 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1221+9T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2595630 | |||||||
| chr18:2595780 | A | G | 1 | a0005c0006t0001g0353 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1221+159A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2595780 | |||||||
| chr18:2595854 | C | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+233C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2595854 | |||||||
| chr18:2595946 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1221+325G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2595946 | |||||||
| chr18:2595990 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+369A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2595990 | |||||||
| chr18:2596115 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1221+494C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596115 | |||||||
| chr18:2596185 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(15): Show |
20 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.1221+564A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596185 | |||||||
| chr18:2596214 | T | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1221+593T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596214 | |||||||
| chr18:2596283 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 |
3 | HG02257.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1221+662A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596283 | |||||||
| chr18:2596284 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1221+663A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596284 | |||||||
| chr18:2596344 | A | C | 1 | a0001c0001t0001g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1221+723A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596344 | |||||||
| chr18:2596418 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221+797T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596418 | |||||||
| chr18:2596504 | G | A | 366 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(363): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.1221+883G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596504 | |||||||
| chr18:2596565 | G | T | 8 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0114 others(5): Show |
8 | NA18953.hp2 NA18955.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1221+944G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596565 | |||||||
| chr18:2596619 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1221+998G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596619 | |||||||
| chr18:2596709 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1221+1088A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596709 | |||||||
| chr18:2596726 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1221+1105C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596726 | |||||||
| chr18:2596846 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
152 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1221+1225G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596846 | |||||||
| chr18:2596883 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1221+1262G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596883 | |||||||
| chr18:2596961 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0031 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1221+1340G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596961 | |||||||
| chr18:2596979 | G | A | 3 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 |
3 | NA19003.hp1 NA19006.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1221+1358G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2596979 | |||||||
| chr18:2597099 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1221+1478A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597099 | |||||||
| chr18:2597192 | TAAATA | T | 3 | a0002c0002t0001g0351 a0002c0002t0001g0352 a0002c0002t0001g0369 |
3 | NA19059.hp2 NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1221+1592_1221+159 others(9): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr18 | 2597192 | ||||||
| chr18:2597211 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1221+1590T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597211 | |||||||
| chr18:2597446 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1222-1573T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597446 | |||||||
| chr18:2597529 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0136 a0001c0001t0001g0137 |
4 | HG02615.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-1490G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597529 | |||||||
| chr18:2597614 | G | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1222-1405G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597614 | |||||||
| chr18:2597638 | G | A | 4 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-1381G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597638 | |||||||
| chr18:2597656 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0170 |
2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1222-1363G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597656 | |||||||
| chr18:2597721 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
98 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1222-1298A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597721 | |||||||
| chr18:2597729 | T | TA | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
50 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.1222-1277dupA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr18 | 2597729 | ||||||
| chr18:2597729 | TA | T | 193 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(190): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1222-1277delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr18 | 2597729 | ||||||
| chr18:2597916 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1222-1103A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597916 | |||||||
| chr18:2597941 | G | A | 1 | a0003c0003t0001g0091 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1222-1078G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2597941 | |||||||
| chr18:2598059 | CATTTAAT others(20): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1222-940_1222-914d others(29): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr18 | 2598059 | ||||||
| chr18:2598084 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1222-935A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598084 | |||||||
| chr18:2598156 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1222-863G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598156 | |||||||
| chr18:2598196 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1222-823A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598196 | |||||||
| chr18:2598421 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1222-598T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598421 | |||||||
| chr18:2598556 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1222-463A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598556 | |||||||
| chr18:2598605 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0143 |
3 | HG01070.hp2 HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1222-414A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598605 | |||||||
| chr18:2598613 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1222-406A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598613 | |||||||
| chr18:2598619 | T | C | 1 | a0003c0003t0001g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1222-400T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598619 | |||||||
| chr18:2598730 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0054 |
3 | HG01934.hp1 HG02015.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1222-289A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598730 | |||||||
| chr18:2598874 | C | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1222-145C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598874 | |||||||
| chr18:2598939 | T | A | 1 | a0002c0002t0001g0335 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1222-80T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 11/16 | chr18 | 2598939 | |||||||
| chr18:2599178 | A | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1374+7A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599178 | |||||||
| chr18:2599240 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0143 a0001c0001t0001g0154 others(2): Show |
6 | HG01070.hp2 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.1374+69T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599240 | |||||||
| chr18:2599306 | G | A | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1374+135G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599306 | |||||||
| chr18:2599564 | C | G | 1 | a0002c0002t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1374+393C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599564 | |||||||
| chr18:2599570 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1374+399T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599570 | |||||||
| chr18:2599847 | A | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1374+676A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599847 | |||||||
| chr18:2599940 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(72): Show |
87 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1374+769A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2599940 | |||||||
| chr18:2600150 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1374+979A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600150 | |||||||
| chr18:2600237 | CATA | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0136 others(2): Show |
7 | HG02615.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1374+1073_1374+107 others(7): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr18 | 2600237 | ||||||
| chr18:2600258 | T | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(32): Show |
38 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.1374+1087T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600258 | |||||||
| chr18:2600357 | T | C | 1 | a0002c0002t0001g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1375-1039T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600357 | |||||||
| chr18:2600361 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1375-1035A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600361 | |||||||
| chr18:2600502 | G | A | 1 | a0003c0003t0001g0266 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1375-894G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600502 | |||||||
| chr18:2600506 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1375-890G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600506 | |||||||
| chr18:2600524 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0226 a0001c0001t0001g0231 |
3 | HG01361.hp1 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1375-872G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600524 | |||||||
| chr18:2600569 | C | G | 94 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
100 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1375-827C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600569 | |||||||
| chr18:2600801 | G | A | 212 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1375-595G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600801 | |||||||
| chr18:2600967 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-429A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2600967 | |||||||
| chr18:2601093 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1375-303A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2601093 | |||||||
| chr18:2601108 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1375-288C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2601108 | |||||||
| chr18:2601118 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1375-278T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2601118 | |||||||
| chr18:2601161 | G | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0346 |
2 | NA18994.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1375-235G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 12/16 | chr18 | 2601161 | |||||||
| chr18:2601516 | A | G | 12 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0042 others(9): Show |
12 | HG01192.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464+31A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2601516 | |||||||
| chr18:2601623 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1464+138T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2601623 | |||||||
| chr18:2601682 | A | G | 1 | a0002c0002t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1464+197A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2601682 | |||||||
| chr18:2601771 | A | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1464+286A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2601771 | |||||||
| chr18:2601986 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1464+501T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2601986 | |||||||
| chr18:2602196 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1464+711A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602196 | |||||||
| chr18:2602224 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1464+739T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602224 | |||||||
| chr18:2602430 | A | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1464+945A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602430 | |||||||
| chr18:2602749 | A | G | 1 | a0003c0003t0001g0264 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1464+1264A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602749 | |||||||
| chr18:2602838 | A | T | 1 | a0001c0001t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1464+1353A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602838 | |||||||
| chr18:2602905 | G | A | 1 | a0002c0002t0001g0333 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1464+1420G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602905 | |||||||
| chr18:2602963 | TGAG | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00099.hp1 HG01069.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1464+1482_1464+148 others(7): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2602963 | ||||||
| chr18:2602969 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1464+1484G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2602969 | |||||||
| chr18:2603069 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1464+1584G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603069 | |||||||
| chr18:2603134 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1464+1649A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603134 | |||||||
| chr18:2603351 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0319 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1464+1870_1464+187 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0317 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1464+1870_1464+187 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(7): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0318 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1464+1870_1464+187 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0322 |
2 | HG02145.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1464+1870_1464+187 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0316 |
3 | HG02280.hp1 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1464+1870_1464+187 others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1464+1870_1464+187 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603351 | T | TTATATAT others(15): Show |
2 | a0001c0001t0001g0320 a0001c0001t0001g0323 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1464+1870_1464+187 others(26): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603351 | ||||||
| chr18:2603356 | C | CAT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0090 others(14): Show |
19 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1464+1893_1464+189 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATAT | 5 | a0001c0001t0001g0052 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG00099.hp2 HG01243.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464+1889_1464+189 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(3): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0053 others(13): Show |
18 | HG00438.hp2 HG00597.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1464+1885_1464+189 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(5): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0003g0032 |
3 | HG03209.hp2 NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1464+1883_1464+189 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(7): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0037 others(3): Show |
6 | HG02074.hp2 HG02132.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1464+1881_1464+189 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(11): Show |
3 | a0002c0002t0001g0330 a0002c0002t0001g0360 a0002c0002t0001g0370 |
3 | HG02145.hp2 HG02647.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1464+1877_1464+189 others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(13): Show |
7 | a0001c0001t0001g0034 a0002c0002t0001g0026 a0002c0002t0001g0326 others(4): Show |
8 | HG01257.hp2 HG01258.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1464+1875_1464+189 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(15): Show |
9 | a0002c0002t0001g0024 a0002c0002t0001g0027 a0002c0002t0001g0324 others(6): Show |
11 | HG00544.hp1 HG01074.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1464+1873_1464+189 others(26): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(17): Show |
7 | a0002c0002t0001g0334 a0002c0002t0001g0347 a0002c0002t0001g0355 others(4): Show |
7 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(28): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(19): Show |
8 | a0002c0002t0001g0040 a0002c0002t0001g0327 a0002c0002t0001g0329 others(5): Show |
8 | HG00738.hp2 HG02559.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(30): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(21): Show |
10 | a0001c0001t0001g0084 a0002c0002t0001g0042 a0002c0002t0001g0325 others(7): Show |
10 | HG02165.hp2 HG02451.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(32): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(23): Show |
3 | a0001c0001t0001g0033 a0002c0002t0001g0085 a0002c0002t0001g0344 |
3 | HG02055.hp2 HG02135.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(34): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(25): Show |
6 | a0001c0001t0001g0035 a0002c0002t0001g0039 a0002c0002t0001g0043 others(3): Show |
6 | HG01496.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(36): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(29): Show |
4 | a0002c0002t0001g0025 a0002c0002t0001g0046 a0002c0002t0001g0047 others(1): Show |
5 | HG00735.hp2 HG01175.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(40): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | CATATATA others(33): Show |
2 | a0002c0002t0001g0044 a0002c0002t0002g0048 |
2 | HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1464+1894_1464+189 others(44): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | C | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1464+1871C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603356 | |||||||
| chr18:2603356 | CAT | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
97 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1464+1893_1464+189 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | CATAT | C | 3 | a0002c0002t0001g0365 a0002c0002t0001g0366 a0002c0002t0001g0367 |
3 | HG02258.hp2 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1464+1891_1464+189 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603356 | CATATATA others(1): Show |
C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1464+1887_1464+189 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2603356 | ||||||
| chr18:2603379 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1464+1894_1464+189 others(29): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603379 | |||||||
| chr18:2603380 | C | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1464+1895C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603380 | |||||||
| chr18:2603577 | T | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1464+2092T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603577 | |||||||
| chr18:2603591 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1464+2106T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603591 | |||||||
| chr18:2603822 | A | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1464+2337A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2603822 | |||||||
| chr18:2604110 | G | A | 2 | a0002c0002t0001g0042 a0002c0002t0001g0043 |
2 | HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1465-2305G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604110 | |||||||
| chr18:2604218 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0037 others(17): Show |
22 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1465-2197C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604218 | |||||||
| chr18:2604241 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(8): Show |
19 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1465-2174A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604241 | |||||||
| chr18:2604281 | C | A | 51 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(48): Show |
55 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1465-2134C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604281 | |||||||
| chr18:2604353 | G | T | 1 | a0002c0002t0001g0359 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1465-2062G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604353 | |||||||
| chr18:2604595 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1465-1820T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604595 | |||||||
| chr18:2604793 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1465-1622G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604793 | |||||||
| chr18:2604815 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0111 others(5): Show |
9 | HG00558.hp2 HG02027.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.1465-1600T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2604815 | |||||||
| chr18:2605137 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1465-1278C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605137 | |||||||
| chr18:2605257 | TCGGG | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1465-1152_1465-114 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605257 | ||||||
| chr18:2605262 | CGGGCTAT others(17): Show |
C | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1465-1152_1465-112 others(28): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605262 | |||||||
| chr18:2605262 | CGGGCTAT others(21): Show |
C | 2 | a0001c0001t0001g0031 a0001c0001t0004g0029 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1465-1152_1465-112 others(32): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605262 | |||||||
| chr18:2605263 | G | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1152G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605263 | |||||||
| chr18:2605264 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1151G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605264 | |||||||
| chr18:2605265 | G | T | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1150G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605265 | |||||||
| chr18:2605266 | C | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1149C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605266 | |||||||
| chr18:2605268 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1147A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605268 | |||||||
| chr18:2605270 | ATGTATGT others(7): Show |
A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-1141_1465-112 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605270 | ||||||
| chr18:2605270 | ATGTATGT others(11): Show |
A | 2 | a0001c0001t0001g0068 a0001c0001t0003g0032 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1465-1141_1465-112 others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605270 | ||||||
| chr18:2605274 | A | ATG | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0112 others(13): Show |
17 | HG00597.hp1 HG01516.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1465-1087_1465-108 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | ATGTG | 3 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0004c0004t0001g0147 |
3 | HG00639.hp2 HG01106.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1465-1089_1465-108 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | ATGTGTG | 10 | a0001c0001t0001g0023 a0001c0001t0001g0090 a0001c0001t0001g0121 others(7): Show |
10 | HG03139.hp2 HG03209.hp1 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.1465-1091_1465-108 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0157 a0001c0001t0001g0160 others(2): Show |
5 | HG01255.hp2 HG01261.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-1093_1465-108 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1465-1095_1465-108 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1465-1099_1465-108 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | A | G | 6 | a0001c0001t0001g0113 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02145.hp1 NA18953.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1465-1141A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605274 | |||||||
| chr18:2605274 | ATG | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0018 others(44): Show |
48 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1465-1087_1465-108 others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTG | A | 46 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0106 others(43): Show |
46 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1465-1089_1465-108 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTG | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0016 others(54): Show |
60 | HG00280.hp1 HG00558.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1465-1091_1465-108 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(1): Show |
A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0163 a0001c0001t0001g0172 others(18): Show |
22 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1465-1093_1465-108 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(3): Show |
A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(17): Show |
24 | HG00673.hp1 HG01074.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1465-1095_1465-108 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(5): Show |
A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(51): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.1465-1097_1465-108 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(7): Show |
A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(17): Show |
23 | HG00438.hp2 HG00597.hp2 HG01981.hp2 others(20): Show |
intron_variant | MODIFIER | c.1465-1099_1465-108 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(9): Show |
A | 8 | a0001c0001t0001g0059 a0002c0002t0001g0334 a0002c0002t0001g0340 others(5): Show |
8 | HG00423.hp1 HG00609.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1465-1101_1465-108 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(11): Show |
A | 1 | a0002c0002t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1465-1103_1465-108 others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(13): Show |
A | 2 | a0002c0002t0001g0040 a0002c0002t0001g0044 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1465-1105_1465-108 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(15): Show |
A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0107 |
2 | HG02055.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1465-1107_1465-108 others(26): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605274 | ATGTGTGT others(21): Show |
A | 1 | a0001c0001t0001g0224 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1465-1113_1465-108 others(32): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605274 | ||||||
| chr18:2605282 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0228 |
2 | HG01261.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1465-1133G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605282 | |||||||
| chr18:2605284 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1465-1131G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605284 | |||||||
| chr18:2605288 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1465-1127G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605288 | |||||||
| chr18:2605290 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1465-1125G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605290 | |||||||
| chr18:2605292 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0004g0029 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1465-1123G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605292 | |||||||
| chr18:2605294 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0004g0029 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1465-1121G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605294 | |||||||
| chr18:2605300 | G | T | 1 | a0001c0001t0001g0169 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1465-1115G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605300 | |||||||
| chr18:2605309 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1465-1106T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605309 | |||||||
| chr18:2605320 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0076 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1465-1091_1465-108 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605320 | ||||||
| chr18:2605322 | GTGTGTGT others(1): Show |
G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG01081.hp1 HG01167.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-1089_1465-108 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605322 | ||||||
| chr18:2605324 | GTGTGTA | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG00099.hp1 HG01243.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-1087_1465-108 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605324 | ||||||
| chr18:2605326 | GTGTA | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0069 others(3): Show |
6 | HG00741.hp2 HG01433.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-1084_1465-108 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605326 | ||||||
| chr18:2605330 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG02451.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1465-1085A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605330 | |||||||
| chr18:2605463 | A | G | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1465-952A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605463 | |||||||
| chr18:2605489 | G | C | 1 | a0001c0001t0001g0301 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1465-926G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605489 | |||||||
| chr18:2605511 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-904G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605511 | |||||||
| chr18:2605550 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1465-865A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605550 | |||||||
| chr18:2605562 | C | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-853C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605562 | |||||||
| chr18:2605577 | C | A | 1 | a0001c0001t0001g0288 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1465-838C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605577 | |||||||
| chr18:2605684 | AT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(30): Show |
37 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1465-722delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605684 | ||||||
| chr18:2605722 | TA | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0054 a0001c0001t0001g0174 |
4 | HG01257.hp1 HG01934.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-685delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2605722 | ||||||
| chr18:2605733 | C | G | 1 | a0002c0002t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1465-682C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605733 | |||||||
| chr18:2605754 | C | A | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1465-661C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605754 | |||||||
| chr18:2605937 | T | C | 52 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1465-478T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2605937 | |||||||
| chr18:2606058 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(19): Show |
25 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1465-357T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2606058 | |||||||
| chr18:2606071 | CTAAA | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(19): Show |
25 | HG00438.hp2 HG00597.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1465-339_1465-336d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr18 | 2606071 | ||||||
| chr18:2606250 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1465-165T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2606250 | |||||||
| chr18:2606277 | A | G | 1 | a0002c0002t0001g0352 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1465-138A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 13/16 | chr18 | 2606277 | |||||||
| chr18:2606519 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1557+12G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606519 | |||||||
| chr18:2606534 | G | A | 9 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0114 others(6): Show |
9 | HG00140.hp2 NA18953.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1557+27G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606534 | |||||||
| chr18:2606597 | CTT | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1557+92_1557+93del others(2): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2606597 | ||||||
| chr18:2606819 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1557+312T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606819 | |||||||
| chr18:2606829 | T | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1557+322T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606829 | |||||||
| chr18:2606859 | A | C | 1 | a0002c0002t0001g0324 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1557+352A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606859 | |||||||
| chr18:2606939 | C | T | 1 | a0001c0005t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+432C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2606939 | |||||||
| chr18:2607055 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1557+548A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2607055 | |||||||
| chr18:2607388 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1557+881T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2607388 | |||||||
| chr18:2607819 | A | ACAAACAT others(3731): Show |
1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1558-864_1558-863i others(3740): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607819 | ||||||
| chr18:2607838 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-862A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2607838 | |||||||
| chr18:2607965 | G | GTA | 19 | a0001c0001t0001g0037 a0001c0001t0001g0058 a0001c0001t0001g0065 others(16): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1558-702_1558-701d others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATA | 21 | a0001c0001t0001g0038 a0001c0001t0001g0053 a0001c0001t0001g0071 others(18): Show |
21 | HG01081.hp1 HG01167.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1558-704_1558-701d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(31): Show |
42 | HG00140.hp1 HG01074.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.1558-706_1558-701d others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(1): Show |
37 | a0001c0001t0001g0005 a0001c0001t0001g0170 a0001c0001t0001g0175 others(34): Show |
40 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.1558-708_1558-701d others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(3): Show |
37 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(34): Show |
40 | HG00280.hp2 HG00621.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1558-710_1558-701d others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(5): Show |
43 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0028 others(40): Show |
46 | HG00280.hp1 HG00558.hp1 HG01433.hp2 others(43): Show |
intron_variant | MODIFIER | c.1558-712_1558-701d others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(7): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0086 others(22): Show |
27 | HG00642.hp1 HG00741.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1558-714_1558-701d others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(9): Show |
9 | a0001c0001t0001g0181 a0001c0001t0001g0186 a0001c0001t0001g0197 others(6): Show |
9 | HG02258.hp2 HG02630.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-716_1558-701d others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(11): Show |
8 | a0001c0001t0001g0173 a0001c0001t0001g0182 a0001c0001t0001g0273 others(5): Show |
8 | HG00609.hp2 HG03195.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.1558-718_1558-701d others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1558-720_1558-701d others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0201 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1558-722_1558-701d others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTA | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(18): Show |
24 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.1558-702_1558-701d others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATA | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0102 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1558-704_1558-701d others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0309 a0001c0001t0003g0032 |
6 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-710_1558-701d others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATATAT others(5): Show |
G | 3 | a0002c0002t0001g0334 a0002c0002t0001g0355 a0002c0002t0001g0362 |
3 | HG00423.hp1 HG00609.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1558-712_1558-701d others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0001g0169 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1558-714_1558-701d others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-716_1558-701d others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607965 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0001g0021 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1558-720_1558-701d others(22): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607965 | ||||||
| chr18:2607979 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0295 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1558-720_1558-702d others(21): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607979 | ||||||
| chr18:2607979 | A | ATG | 3 | a0003c0003t0001g0248 a0003c0003t0001g0251 a0003c0003t0001g0252 |
3 | HG01106.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1558-720_1558-719i others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607979 | ||||||
| chr18:2607998 | T | A | 10 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0118 others(7): Show |
10 | HG00735.hp1 HG01106.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-702T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2607998 | |||||||
| chr18:2607998 | T | TAA | 28 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0109 others(25): Show |
29 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.1558-701_1558-700d others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2607998 | T | TATAA | 5 | a0001c0001t0001g0116 a0001c0001t0001g0253 a0003c0003t0001g0007 others(2): Show |
6 | HG01169.hp2 HG01952.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.1558-701_1558-700i others(6): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2607998 | T | TATATAA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0105 others(6): Show |
10 | HG00558.hp2 HG00673.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-701_1558-700i others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2607998 | T | TATATATA others(3): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0127 a0003c0003t0001g0262 |
3 | HG02602.hp1 NA18955.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1558-701_1558-700i others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2607998 | T | TATATATA others(5): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0125 others(1): Show |
4 | HG02027.hp1 NA19054.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1558-701_1558-700i others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2607998 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0126 |
2 | NA18953.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1558-701_1558-700i others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr18 | 2607998 | ||||||
| chr18:2608052 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1558-648A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608052 | |||||||
| chr18:2608105 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558-595C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608105 | |||||||
| chr18:2608213 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1558-487C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608213 | |||||||
| chr18:2608237 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
113 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1558-463G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608237 | |||||||
| chr18:2608245 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1558-455G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608245 | |||||||
| chr18:2608404 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1558-296C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608404 | |||||||
| chr18:2608408 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1558-292G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608408 | |||||||
| chr18:2608410 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1558-290T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608410 | |||||||
| chr18:2608483 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1558-217G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608483 | |||||||
| chr18:2608505 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0031 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1558-195C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608505 | |||||||
| chr18:2608540 | G | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0004g0029 |
3 | HG02257.hp2 HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1558-160G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608540 | |||||||
| chr18:2608628 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1558-72T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608628 | |||||||
| chr18:2608642 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-58C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608642 | |||||||
| chr18:2608682 | G | A | 2 | a0002c0002t0001g0040 a0002c0002t0001g0044 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1558-18G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 14/16 | chr18 | 2608682 | |||||||
| chr18:2608899 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1688+69G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2608899 | |||||||
| chr18:2609110 | A | T | 52 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(49): Show |
56 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1688+280A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609110 | |||||||
| chr18:2609179 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1688+349T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609179 | |||||||
| chr18:2609294 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1688+464T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609294 | |||||||
| chr18:2609338 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1688+508C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609338 | |||||||
| chr18:2609399 | A | T | 1 | a0002c0002t0001g0332 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1688+569A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609399 | |||||||
| chr18:2609460 | A | T | 1 | a0001c0001t0001g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1688+630A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609460 | |||||||
| chr18:2609609 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1688+779C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609609 | |||||||
| chr18:2609635 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1688+805A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609635 | |||||||
| chr18:2609680 | C | CATTCTCA others(5): Show |
1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+850_1688+851i others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609680 | |||||||
| chr18:2609681 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+851T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609681 | |||||||
| chr18:2609686 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+856A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609686 | |||||||
| chr18:2609687 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+857C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609687 | |||||||
| chr18:2609689 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+859G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609689 | |||||||
| chr18:2609690 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+860A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609690 | |||||||
| chr18:2609694 | A | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1688+864A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609694 | |||||||
| chr18:2609707 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+877A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609707 | |||||||
| chr18:2609708 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+878G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609708 | |||||||
| chr18:2609710 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+880A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609710 | |||||||
| chr18:2609716 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+886G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609716 | |||||||
| chr18:2609724 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+894A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609724 | |||||||
| chr18:2609727 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+897T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609727 | |||||||
| chr18:2609728 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+898G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609728 | |||||||
| chr18:2609729 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+899G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609729 | |||||||
| chr18:2609730 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+900G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609730 | |||||||
| chr18:2609734 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+904G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609734 | |||||||
| chr18:2609736 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+906A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609736 | |||||||
| chr18:2609737 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+907A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609737 | |||||||
| chr18:2609740 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+910G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609740 | |||||||
| chr18:2609741 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+911C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609741 | |||||||
| chr18:2609742 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+912A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609742 | |||||||
| chr18:2609759 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+929C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609759 | |||||||
| chr18:2609762 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+932G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609762 | |||||||
| chr18:2609763 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+933T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609763 | |||||||
| chr18:2609764 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+934G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609764 | |||||||
| chr18:2609765 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+935G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609765 | |||||||
| chr18:2609766 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+936C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609766 | |||||||
| chr18:2609768 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+938C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609768 | |||||||
| chr18:2609769 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+939A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609769 | |||||||
| chr18:2609769 | A | G | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1688+939A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609769 | |||||||
| chr18:2609771 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+941T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609771 | |||||||
| chr18:2609776 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+946A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609776 | |||||||
| chr18:2609788 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+958G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609788 | |||||||
| chr18:2609789 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+959A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609789 | |||||||
| chr18:2609790 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+960G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609790 | |||||||
| chr18:2609792 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+962A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609792 | |||||||
| chr18:2609794 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1688+964C>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609794 | |||||||
| chr18:2609796 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1689-963G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609796 | |||||||
| chr18:2609799 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1689-960G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609799 | |||||||
| chr18:2609800 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1689-959T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609800 | |||||||
| chr18:2609801 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1689-958A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609801 | |||||||
| chr18:2609803 | A | G | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-956A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609803 | |||||||
| chr18:2609903 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1689-856A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609903 | |||||||
| chr18:2609931 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1689-828C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2609931 | |||||||
| chr18:2610212 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-547G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610212 | |||||||
| chr18:2610213 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0031 |
2 | HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1689-546T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610213 | |||||||
| chr18:2610324 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | NA19062.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1689-435C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610324 | |||||||
| chr18:2610346 | G | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0030 others(14): Show |
19 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.1689-413G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610346 | |||||||
| chr18:2610481 | A | G | 1 | a0001c0001t0001g0002 | 4 | HG02451.hp1 HG02615.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1689-278A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610481 | |||||||
| chr18:2610530 | T | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0195 a0001c0001t0001g0199 others(5): Show |
9 | HG00738.hp1 HG01081.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1689-229T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610530 | |||||||
| chr18:2610539 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1689-220G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 15/16 | chr18 | 2610539 | |||||||
| chr18:2610979 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1791+118G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2610979 | |||||||
| chr18:2611045 | A | AT | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(225): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1791+204dupT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2611045 | ||||||
| chr18:2611045 | A | ATT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0166 a0001c0001t0001g0172 others(4): Show |
7 | HG00609.hp2 HG01175.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1791+203_1791+204d others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2611045 | ||||||
| chr18:2611045 | AT | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(71): Show |
85 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1791+204delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2611045 | ||||||
| chr18:2611047 | T | C | 1 | a0002c0002t0001g0360 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1791+186T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611047 | |||||||
| chr18:2611301 | G | A | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0034 others(15): Show |
20 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1791+440G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611301 | |||||||
| chr18:2611471 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
97 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1791+610A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611471 | |||||||
| chr18:2611602 | T | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1791+741T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611602 | |||||||
| chr18:2611719 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1791+858G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611719 | |||||||
| chr18:2611877 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1791+1016G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611877 | |||||||
| chr18:2611896 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1791+1035T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2611896 | |||||||
| chr18:2612080 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1791+1219T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612080 | |||||||
| chr18:2612276 | C | CT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0137 a0001c0001t0001g0140 others(4): Show |
8 | HG03130.hp2 HG03225.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1448dupT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | C | CTTTT | 5 | a0001c0001t0001g0014 a0002c0002t0001g0043 a0002c0002t0001g0046 others(2): Show |
6 | HG01243.hp1 HG01496.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+1445_1791+144 others(8): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CT | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0090 a0001c0001t0001g0142 others(14): Show |
18 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1791+1448delT | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTT | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
78 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1791+1443_1791+144 others(10): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(44): Show |
48 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.1791+1442_1791+144 others(11): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT others(1): Show |
C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(178): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1791+1441_1791+144 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT others(2): Show |
C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0086 a0001c0001t0001g0174 others(7): Show |
10 | HG01069.hp1 HG01257.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1440_1791+144 others(13): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0028 a0001c0001t0004g0029 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1791+1439_1791+144 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0068 a0001c0001t0003g0032 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1791+1438_1791+144 others(15): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612276 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0309 |
7 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1437_1791+144 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2612276 | ||||||
| chr18:2612352 | C | T | 68 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0104 others(65): Show |
71 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1791+1491C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612352 | |||||||
| chr18:2612359 | G | A | 94 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0019 others(91): Show |
100 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1791+1498G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612359 | |||||||
| chr18:2612375 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1791+1514G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612375 | |||||||
| chr18:2612449 | C | T | 2 | a0002c0002t0001g0040 a0002c0002t0001g0044 |
2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1791+1588C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612449 | |||||||
| chr18:2612532 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1791+1671G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612532 | |||||||
| chr18:2612579 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1791+1718C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612579 | |||||||
| chr18:2612587 | A | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1791+1726A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612587 | |||||||
| chr18:2612593 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1732T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612593 | |||||||
| chr18:2612658 | T | C | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0322 |
3 | HG02109.hp1 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1791+1797T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612658 | |||||||
| chr18:2612740 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1879A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612740 | |||||||
| chr18:2612952 | T | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0003g0032 others(1): Show |
4 | HG02257.hp2 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+2091T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612952 | |||||||
| chr18:2612992 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(57): Show |
71 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1791+2131G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2612992 | |||||||
| chr18:2613235 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1791+2374T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613235 | |||||||
| chr18:2613426 | T | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0083 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2565T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613426 | |||||||
| chr18:2613442 | A | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0302 |
2 | NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1791+2581A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613442 | |||||||
| chr18:2613540 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1791+2679G>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613540 | |||||||
| chr18:2613732 | CAAATTTA others(7): Show |
C | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1792-2704_1792-269 others(18): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613732 | |||||||
| chr18:2613778 | A | G | 14 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0102 others(11): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1792-2659A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613778 | |||||||
| chr18:2613779 | C | T | 16 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0068 others(13): Show |
18 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1792-2658C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613779 | |||||||
| chr18:2613842 | A | G | 1 | a0001c0001t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1792-2595A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613842 | |||||||
| chr18:2613851 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1792-2586C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613851 | |||||||
| chr18:2613897 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(60): Show |
75 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1792-2540A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613897 | |||||||
| chr18:2613997 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-2440T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2613997 | |||||||
| chr18:2614148 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(311): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1792-2289C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614148 | |||||||
| chr18:2614160 | T | C | 1 | a0001c0001t0001g0001 | 4 | HG01074.hp2 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-2277T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614160 | |||||||
| chr18:2614214 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-2223G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614214 | |||||||
| chr18:2614392 | G | A | 27 | a0003c0003t0001g0007 a0003c0003t0001g0008 a0003c0003t0001g0091 others(24): Show |
29 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1792-2045G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614392 | |||||||
| chr18:2614407 | A | C | 1 | a0002c0002t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-2030A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614407 | |||||||
| chr18:2614434 | TCAAAAAA others(1): Show |
T | 3 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0001g0049 |
3 | HG01496.hp2 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1792-2002_1792-199 others(12): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614434 | |||||||
| chr18:2614434 | TCAAAAAA others(9): Show |
T | 3 | a0002c0002t0001g0039 a0002c0002t0001g0046 a0002c0002t0001g0050 |
3 | HG02257.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1792-2002_1792-198 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614434 | |||||||
| chr18:2614434 | TCAAAAAA others(13): Show |
T | 1 | a0002c0002t0002g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1792-2002_1792-198 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614434 | |||||||
| chr18:2614435 | C | G | 5 | a0002c0002t0001g0040 a0002c0002t0001g0044 a0002c0002t0001g0047 others(2): Show |
5 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-2002C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614435 | |||||||
| chr18:2614439 | A | AAAAGAAA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1792-1965_1792-195 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614439 | A | AAAAGAAA others(9): Show |
1 | a0001c0001t0001g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1792-1969_1792-195 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614439 | A | AAAAGAAA others(49): Show |
1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(60): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614439 | A | AAAAGAAA others(73): Show |
1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(84): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614439 | A | G | 7 | a0001c0001t0001g0162 a0001c0001t0001g0277 a0002c0002t0001g0040 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-1998A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614439 | |||||||
| chr18:2614439 | AAAAGAAA others(147): Show |
A | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1792-1953_1792-180 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614439 | AAAAGAAA others(163): Show |
A | 1 | a0001c0005t0001g0138 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1792-1953_1792-178 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614439 | ||||||
| chr18:2614440 | A | AAAGAAAG others(8): Show |
1 | a0001c0001t0001g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1792-1994_1792-198 others(19): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614440 | ||||||
| chr18:2614440 | AAAGAAAG others(170): Show |
A | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1792-1994_1792-181 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614440 | ||||||
| chr18:2614441 | AAGAAAGA others(173): Show |
A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-1994_1792-181 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614441 | ||||||
| chr18:2614442 | AGAAAGAA others(176): Show |
A | 1 | a0001c0001t0001g0287 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1792-1994_1792-181 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614442 | |||||||
| chr18:2614443 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1792-1994G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614443 | |||||||
| chr18:2614443 | G | GAAAGAAA others(17): Show |
1 | a0001c0001t0001g0279 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1792-1971_1792-197 others(28): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614443 | ||||||
| chr18:2614453 | A | AGAGAGAG others(14): Show |
1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1984_1792-198 others(25): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614453 | |||||||
| chr18:2614456 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0002c0002t0001g0051 |
3 | HG01243.hp1 HG02257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1792-1981A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614456 | |||||||
| chr18:2614457 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1980A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614457 | |||||||
| chr18:2614459 | GAAAGAAA others(191): Show |
G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0015 others(37): Show |
45 | HG00438.hp2 HG00597.hp2 HG01167.hp2 others(42): Show |
intron_variant | MODIFIER | c.1792-1974_1792-177 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614459 | ||||||
| chr18:2614460 | A | G | 2 | a0002c0002t0001g0051 a0002c0002t0002g0048 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1792-1977A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614460 | |||||||
| chr18:2614461 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1792-1976A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614461 | |||||||
| chr18:2614461 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1976A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614461 | |||||||
| chr18:2614463 | GAAAGAAA others(187): Show |
G | 4 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1970_1792-177 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614463 | ||||||
| chr18:2614464 | A | G | 3 | a0002c0002t0001g0047 a0002c0002t0001g0051 a0002c0002t0002g0048 |
3 | HG01192.hp2 HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1792-1973A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614464 | |||||||
| chr18:2614465 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0004g0029 |
2 | HG03225.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1792-1972A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614465 | |||||||
| chr18:2614468 | A | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0002c0002t0001g0047 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1969A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614468 | |||||||
| chr18:2614468 | AAAGAAAG others(17): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1792-1965_1792-194 others(28): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614468 | ||||||
| chr18:2614469 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1968A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614469 | |||||||
| chr18:2614471 | GAAAGAAA others(179): Show |
G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1792-1962_1792-177 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614471 | ||||||
| chr18:2614472 | A | G | 6 | a0001c0001t0001g0013 a0002c0002t0001g0047 a0002c0002t0001g0049 others(3): Show |
6 | HG01070.hp2 HG01192.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1965A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614472 | |||||||
| chr18:2614472 | AAAGAAAG others(13): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1792-1961_1792-194 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614472 | ||||||
| chr18:2614472 | AAAGAAAG others(29): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1792-1961_1792-192 others(40): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614472 | ||||||
| chr18:2614473 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1964A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614473 | |||||||
| chr18:2614475 | GAAAGAAA others(175): Show |
G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(33): Show |
40 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1792-1958_1792-177 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614475 | ||||||
| chr18:2614476 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0137 a0002c0002t0001g0042 others(5): Show |
9 | HG01070.hp2 HG01192.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792-1961A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614476 | |||||||
| chr18:2614477 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1960A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614477 | |||||||
| chr18:2614479 | GAAAGGAA others(171): Show |
G | 28 | a0001c0001t0001g0019 a0003c0003t0001g0007 a0003c0003t0001g0008 others(25): Show |
30 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.1792-1954_1792-177 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614479 | ||||||
| chr18:2614480 | A | AAAGAAAG others(61): Show |
1 | a0001c0001t0001g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(72): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614480 | ||||||
| chr18:2614480 | A | AAAGAAAG others(65): Show |
1 | a0001c0001t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(76): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614480 | ||||||
| chr18:2614480 | A | AAAGAAAG others(73): Show |
1 | a0001c0001t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(84): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614480 | ||||||
| chr18:2614480 | A | AAAGAAAG others(37): Show |
1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(48): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614480 | ||||||
| chr18:2614480 | A | AAAGAAGA others(25): Show |
1 | a0001c0001t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1792-1954_1792-195 others(36): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614480 | ||||||
| chr18:2614480 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(11): Show |
17 | HG01070.hp2 HG01192.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1792-1957A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614480 | |||||||
| chr18:2614481 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1956A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614481 | |||||||
| chr18:2614483 | GGAAGGAA others(167): Show |
G | 5 | a0003c0003t0001g0248 a0003c0003t0001g0251 a0003c0003t0001g0252 others(2): Show |
5 | HG01106.hp2 HG02559.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-1953_1792-178 others(4): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614483 | |||||||
| chr18:2614484 | G | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0139 others(17): Show |
20 | HG00639.hp2 HG01106.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1792-1953G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614484 | |||||||
| chr18:2614485 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1952A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614485 | |||||||
| chr18:2614488 | G | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0139 others(12): Show |
15 | HG02257.hp2 HG02630.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.1792-1949G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614488 | |||||||
| chr18:2614489 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1948A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614489 | |||||||
| chr18:2614492 | G | A | 8 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0153 others(5): Show |
8 | HG01106.hp1 HG02698.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1945G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614492 | |||||||
| chr18:2614493 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1944A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614493 | |||||||
| chr18:2614496 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0153 others(2): Show |
5 | HG02257.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1941G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614496 | |||||||
| chr18:2614497 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1940A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614497 | |||||||
| chr18:2614500 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0154 a0001c0001t0004g0029 |
3 | HG02257.hp2 HG03225.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1792-1937G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614500 | |||||||
| chr18:2614501 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1936A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614501 | |||||||
| chr18:2614504 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1933G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614504 | |||||||
| chr18:2614505 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1932A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614505 | |||||||
| chr18:2614508 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0004g0029 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1929G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614508 | |||||||
| chr18:2614509 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1928A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614509 | |||||||
| chr18:2614512 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1925G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614512 | |||||||
| chr18:2614513 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1924A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614513 | |||||||
| chr18:2614516 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1921G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614516 | |||||||
| chr18:2614517 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1920A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614517 | |||||||
| chr18:2614520 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1917G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614520 | |||||||
| chr18:2614521 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1916A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614521 | |||||||
| chr18:2614524 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1913G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614524 | |||||||
| chr18:2614525 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1912A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614525 | |||||||
| chr18:2614528 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1909G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614528 | |||||||
| chr18:2614529 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1908A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614529 | |||||||
| chr18:2614531 | GGAAGGAA others(41): Show |
G | 1 | a0001c0001t0001g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1792-1905_1792-185 others(52): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614531 | |||||||
| chr18:2614532 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1905G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614532 | |||||||
| chr18:2614532 | GAAGGAAG others(59): Show |
G | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1792-1901_1792-183 others(70): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614532 | ||||||
| chr18:2614533 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1904A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614533 | |||||||
| chr18:2614534 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1792-1903A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614534 | |||||||
| chr18:2614535 | GGAAGGAA others(66): Show |
G | 1 | a0002c0002t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1792-1898_1792-182 others(77): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614535 | ||||||
| chr18:2614536 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1901G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614536 | |||||||
| chr18:2614537 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1900A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614537 | |||||||
| chr18:2614539 | GGAAGGAA others(25): Show |
G | 1 | a0001c0001t0001g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1792-1897_1792-186 others(36): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614539 | |||||||
| chr18:2614540 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1897G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614540 | |||||||
| chr18:2614540 | GAAGGAAG others(43): Show |
G | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1792-1893_1792-184 others(54): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614540 | ||||||
| chr18:2614541 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1896A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614541 | |||||||
| chr18:2614543 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1792-1894G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614543 | |||||||
| chr18:2614544 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1893G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614544 | |||||||
| chr18:2614545 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1892A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614545 | |||||||
| chr18:2614547 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1792-1890G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614547 | |||||||
| chr18:2614548 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1889G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614548 | |||||||
| chr18:2614549 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1888A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614549 | |||||||
| chr18:2614549 | AAGGAAGG others(13): Show |
A | 1 | a0001c0001t0001g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1792-1886_1792-186 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614549 | ||||||
| chr18:2614551 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01070.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1792-1886G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614551 | |||||||
| chr18:2614552 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1885G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614552 | |||||||
| chr18:2614553 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1884A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614553 | |||||||
| chr18:2614553 | AAGGAAGG others(9): Show |
A | 1 | a0001c0001t0001g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1792-1882_1792-186 others(20): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614553 | ||||||
| chr18:2614553 | AAGGAAGG others(13): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1792-1882_1792-186 others(24): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614553 | ||||||
| chr18:2614555 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01070.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1792-1882G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614555 | |||||||
| chr18:2614555 | G | GAAAGAAA others(64): Show |
1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1792-1882_1792-188 others(75): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614555 | |||||||
| chr18:2614556 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0004g0029 |
2 | HG01517.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1881G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614556 | |||||||
| chr18:2614557 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1880A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614557 | |||||||
| chr18:2614559 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0143 others(1): Show |
4 | HG01070.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1878G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614559 | |||||||
| chr18:2614559 | GGAAGGGA others(42): Show |
G | 1 | a0002c0002t0001g0043 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1792-1874_1792-182 others(53): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614559 | ||||||
| chr18:2614560 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0004g0029 |
2 | HG01517.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1877G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614560 | |||||||
| chr18:2614561 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1876A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614561 | |||||||
| chr18:2614562 | AG | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0143 a0002c0002t0001g0046 others(4): Show |
7 | HG01123.hp2 HG01243.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-1872delG | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614562 | ||||||
| chr18:2614563 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0144 a0001c0001t0001g0149 others(4): Show |
7 | HG01070.hp2 HG01496.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1874G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614563 | |||||||
| chr18:2614563 | G | GAAAGAAA others(27): Show |
1 | a0001c0001t0001g0157 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1792-1874_1792-187 others(38): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614563 | |||||||
| chr18:2614563 | GGGAAAGA others(6): Show |
G | 1 | a0002c0002t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1792-1872_1792-186 others(17): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614563 | ||||||
| chr18:2614563 | GGGAAAGA others(30): Show |
G | 2 | a0002c0002t0001g0042 a0002c0002t0002g0048 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1792-1872_1792-183 others(41): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614563 | ||||||
| chr18:2614564 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
10 | HG01123.hp2 HG01255.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1792-1873G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAAAAAG others(63): Show |
1 | a0001c0001t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(74): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAAAGAA others(5): Show |
1 | a0001c0001t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(16): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAAAGAA others(33): Show |
1 | a0001c0001t0001g0141 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(44): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAAGAAA others(144): Show |
1 | a0001c0001t0001g0013 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(155): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAAGGAA others(108): Show |
1 | a0001c0001t0001g0151 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(119): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGAAAG others(35): Show |
1 | a0001c0001t0001g0158 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(46): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(261): Show |
1 | a0001c0001t0001g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(272): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(276): Show |
1 | a0001c0001t0001g0013 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(287): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(67): Show |
1 | a0001c0001t0001g0281 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(78): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(36): Show |
1 | a0004c0004t0001g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(47): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(25): Show |
1 | a0004c0004t0001g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(36): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(49): Show |
1 | a0001c0001t0001g0278 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(60): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(216): Show |
1 | a0001c0001t0001g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(227): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(61): Show |
1 | a0001c0001t0001g0153 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(72): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(61): Show |
1 | a0001c0001t0001g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(72): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | G | GAAGGAAG others(67): Show |
1 | a0001c0001t0001g0139 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1792-1873_1792-187 others(78): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614564 | GGAAAGAA others(3): Show |
G | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1792-1872_1792-186 others(14): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614564 | |||||||
| chr18:2614565 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0146 others(4): Show |
7 | HG02280.hp2 HG03225.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-1872G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614565 | |||||||
| chr18:2614567 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0004g0029 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1792-1870A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614567 | |||||||
| chr18:2614568 | A | G | 5 | a0002c0002t0001g0046 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-1869A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614568 | |||||||
| chr18:2614571 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1866A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614571 | |||||||
| chr18:2614572 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0049 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1865A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614572 | |||||||
| chr18:2614573 | G | GAAAGAAA others(39): Show |
1 | a0001c0001t0001g0144 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1792-1862_1792-181 others(50): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614573 | ||||||
| chr18:2614574 | A | AAAGAAAG others(32): Show |
1 | a0001c0001t0001g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1792-1860_1792-182 others(43): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614574 | ||||||
| chr18:2614574 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-1863A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614574 | |||||||
| chr18:2614575 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1862A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614575 | |||||||
| chr18:2614576 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0049 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1861A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614576 | |||||||
| chr18:2614578 | A | G | 2 | a0001c0001t0001g0152 a0002c0002t0001g0044 |
2 | HG02717.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1792-1859A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614578 | |||||||
| chr18:2614579 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1858A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614579 | |||||||
| chr18:2614580 | A | G | 7 | a0002c0002t0001g0040 a0002c0002t0001g0046 a0002c0002t0001g0047 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1857A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614580 | |||||||
| chr18:2614582 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-1855A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614582 | |||||||
| chr18:2614583 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1854A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614583 | |||||||
| chr18:2614584 | A | G | 7 | a0002c0002t0001g0040 a0002c0002t0001g0046 a0002c0002t0001g0047 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1853A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614584 | |||||||
| chr18:2614586 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-1851A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614586 | |||||||
| chr18:2614587 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1850A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614587 | |||||||
| chr18:2614588 | A | G | 7 | a0002c0002t0001g0040 a0002c0002t0001g0046 a0002c0002t0001g0047 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1849A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614588 | |||||||
| chr18:2614591 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1846A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614591 | |||||||
| chr18:2614592 | A | G | 7 | a0002c0002t0001g0040 a0002c0002t0001g0046 a0002c0002t0001g0047 others(4): Show |
7 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1845A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614592 | |||||||
| chr18:2614595 | A | G | 2 | a0001c0001t0004g0029 a0002c0002t0001g0040 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1792-1842A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614595 | |||||||
| chr18:2614596 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0049 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1841A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614596 | |||||||
| chr18:2614598 | A | AAAGAAAG others(32): Show |
1 | a0001c0001t0001g0280 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1792-1836_1792-179 others(43): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614598 | ||||||
| chr18:2614599 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1838A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614599 | |||||||
| chr18:2614600 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0047 a0002c0002t0001g0049 others(3): Show |
6 | HG01192.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1837A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614600 | |||||||
| chr18:2614603 | A | G | 3 | a0001c0001t0004g0029 a0002c0002t0001g0042 a0002c0002t0001g0047 |
3 | HG01192.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1834A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614603 | |||||||
| chr18:2614604 | A | AGAAAGAA others(46): Show |
1 | a0001c0001t0001g0282 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1792-1781_1792-178 others(57): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614604 | ||||||
| chr18:2614604 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0049 a0002c0002t0001g0050 others(3): Show |
6 | HG01243.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1833A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614604 | |||||||
| chr18:2614607 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1830A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614607 | |||||||
| chr18:2614608 | A | G | 6 | a0002c0002t0001g0046 a0002c0002t0001g0049 a0002c0002t0001g0050 others(3): Show |
6 | HG01243.hp1 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1829A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614608 | |||||||
| chr18:2614611 | A | G | 6 | a0001c0001t0004g0029 a0002c0002t0001g0039 a0002c0002t0001g0043 others(3): Show |
6 | HG01243.hp1 HG01496.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1826A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614611 | |||||||
| chr18:2614612 | A | G | 3 | a0002c0002t0001g0046 a0002c0002t0002g0045 a0002c0002t0002g0048 |
3 | HG02559.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1792-1825A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614612 | |||||||
| chr18:2614615 | A | G | 3 | a0001c0001t0004g0029 a0002c0002t0001g0046 a0002c0002t0002g0048 |
3 | HG02886.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1822A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614615 | |||||||
| chr18:2614616 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1792-1821A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614616 | |||||||
| chr18:2614617 | G | GAAAGAAA others(55): Show |
1 | a0001c0001t0001g0279 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1792-1804_1792-180 others(66): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614617 | ||||||
| chr18:2614619 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1818A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614619 | |||||||
| chr18:2614620 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1792-1817A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614620 | |||||||
| chr18:2614621 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1792-1816G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614621 | |||||||
| chr18:2614623 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1814A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614623 | |||||||
| chr18:2614624 | A | G | 1 | a0002c0002t0002g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1792-1813A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614624 | |||||||
| chr18:2614625 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-1812G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614625 | |||||||
| chr18:2614627 | A | G | 2 | a0001c0001t0004g0029 a0002c0002t0002g0045 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1792-1810A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614627 | |||||||
| chr18:2614629 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-1808G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614629 | |||||||
| chr18:2614631 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1806A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614631 | |||||||
| chr18:2614633 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-1804G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614633 | |||||||
| chr18:2614635 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1802A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614635 | |||||||
| chr18:2614639 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1798A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614639 | |||||||
| chr18:2614641 | GA | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG01106.hp1 HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1792-1793delA | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614641 | ||||||
| chr18:2614643 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1794A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614643 | |||||||
| chr18:2614647 | A | G | 1 | a0001c0001t0004g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1792-1790A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614647 | |||||||
| chr18:2614649 | G | GAAAGAAA others(90): Show |
1 | a0001c0001t0001g0162 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1792-1781_1792-178 others(101): Show |
NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr18 | 2614649 | ||||||
| chr18:2614657 | T | G | 54 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
58 | HG00639.hp2 HG01070.hp2 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.1792-1780T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614657 | |||||||
| chr18:2614658 | A | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1792-1779A>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614658 | |||||||
| chr18:2614838 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1792-1599T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614838 | |||||||
| chr18:2614884 | G | T | 6 | a0003c0003t0001g0091 a0003c0003t0001g0092 a0003c0003t0001g0093 others(3): Show |
6 | HG00597.hp1 NA18953.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1553G>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614884 | |||||||
| chr18:2614887 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG01070.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1792-1550A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614887 | |||||||
| chr18:2614955 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0065 |
2 | HG02155.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1792-1482G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2614955 | |||||||
| chr18:2615083 | G | A | 1 | a0002c0002t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1792-1354G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615083 | |||||||
| chr18:2615101 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-1336C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615101 | |||||||
| chr18:2615157 | C | T | 1 | a0002c0002t0001g0351 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1792-1280C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615157 | |||||||
| chr18:2615293 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1792-1144T>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615293 | |||||||
| chr18:2615489 | A | C | 4 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-948A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615489 | |||||||
| chr18:2615598 | A | C | 1 | a0002c0002t0001g0370 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1792-839A>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615598 | |||||||
| chr18:2615637 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1792-800T>C | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615637 | |||||||
| chr18:2615735 | C | T | 1 | a0003c0003t0001g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1792-702C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615735 | |||||||
| chr18:2615762 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1792-675C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615762 | |||||||
| chr18:2615797 | A | G | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(328): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1792-640A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615797 | |||||||
| chr18:2615821 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1792-616T>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615821 | |||||||
| chr18:2615844 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-593C>T | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2615844 | |||||||
| chr18:2616081 | A | G | 1 | a0002c0002t0001g0306 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1792-356A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616081 | |||||||
| chr18:2616089 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(192): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1792-348A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616089 | |||||||
| chr18:2616090 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-347A>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616090 | |||||||
| chr18:2616120 | G | A | 1 | a0002c0002t0001g0340 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1792-317G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616120 | |||||||
| chr18:2616290 | G | A | 101 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1792-147G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616290 | |||||||
| chr18:2616321 | G | A | 49 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(46): Show |
53 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1792-116G>A | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616321 | |||||||
| chr18:2616414 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1792-23C>G | NDC80 | ENSG00000080986.13 | transcript | ENST00000261597.9 | protein_coding | 16/16 | chr18 | 2616414 |