Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83540 |
| ensemblid | ENSG00000143228.13 |
| hgncid | 14621 |
| symbol | NUF2 |
| name | NUF2 component of NDC80 kinetochore complex |
| refseq_nuc | NM_145697.3 |
| refseq_prot | NP_663735.2 |
| ensembl_nuc | ENST00000271452.8 |
| ensembl_prot | ENSP00000271452.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 163321954 |
| end | 163355759 |
| strand | + |
| ver | v1.2 |
| region | chr1:163321954-163355759 |
| region5000 | chr1:163316954-163360759 |
| regionname0 | NUF2_chr1_163321954_163355759 |
| regionname5000 | NUF2_chr1_163316954_163360759 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 464 | 340 | 70 | 69 | 152 | 10 | 37 | 111 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0002 | 0/0 | 464 | 40 | 16 | 7 | 10 | 2 | 5 | 8 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0003 | 0/0 | 464 | 8 | 4 | 0 | 4 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0004 | 0/0 | 464 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0005 | 0/0 | 464 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0006 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0007 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0008 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| a0009 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | METLS others(459): Show |
chr1 | 163316954 | 163360759 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1392 | 176 | 24 | 41 | 75 | 8 | 27 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0001c0002 | 1/0 | 1392 | 164 | 46 | 28 | 77 | 2 | 10 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0002c0003 | 0/0 | 1392 | 25 | 6 | 5 | 10 | 2 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0002c0004 | 0/0 | 1392 | 15 | 10 | 2 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0003c0005 | 0/0 | 1392 | 8 | 4 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0004c0006 | 0/0 | 1392 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0005c0007 | 0/0 | 1392 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0006c0009 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0007c0008 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0008c0011 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 | ||
| a0009c0010 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | ATGGA others(1387): Show |
chr1 | 163316954 | 163360759 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1964 | 174 | 24 | 40 | 75 | 8 | 26 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0001c0001t0004 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0001c0001t0005 | 0/0 | 1964 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0001c0002t0001 | 1/0 | 1964 | 161 | 46 | 28 | 76 | 2 | 8 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0001c0002t0002 | 0/0 | 1964 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0001c0002t0003 | 0/0 | 1964 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0002c0003t0001 | 0/0 | 1964 | 25 | 6 | 5 | 10 | 2 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0002c0004t0001 | 0/0 | 1964 | 15 | 10 | 2 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0003c0005t0001 | 0/0 | 1964 | 8 | 4 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0004c0006t0001 | 0/0 | 1964 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0005c0007t0001 | 0/0 | 1964 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0006c0009t0001 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0007c0008t0001 | 0/0 | 1964 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0008c0011t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| a0009c0010t0001 | 0/0 | 1964 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | AGTAG others(1959): Show |
chr1 | 163316954 | 163360759 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 17 | 0 | 2 | 11 | 0 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 2 | 5 | 3 | 4 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0005 | 0/0 | 13 | 3 | 1 | 9 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0011 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0012 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0015 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0026 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0001 | 0/0 | 19 | 0 | 3 | 14 | 0 | 2 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0002 | 0/0 | 18 | 0 | 1 | 17 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0008 | 0/0 | 10 | 0 | 5 | 5 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0009 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0010 | 1/0 | 8 | 7 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0013 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0006 | 0/0 | 13 | 3 | 5 | 2 | 2 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0002c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0003c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0004c0006t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0005c0007t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0006c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0007c0008t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0008c0011t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| a0009c0010t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0006 | EUR | GBR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0006 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00423 | hp1 | a0003 | c0005 | t0001 | g0152 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0022 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00738 | hp2 | a0006 | c0009 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0025 | AMR | PUR | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01257 | hp1 | a0005 | c0007 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01258 | hp1 | a0005 | c0007 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01361 | hp2 | a0007 | c0008 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0037 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | IBS | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01891 | hp2 | a0008 | c0011 | t0001 | g0177 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02004 | hp1 | a0002 | c0004 | t0001 | g0148 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02080 | hp1 | a0003 | c0005 | t0001 | g0151 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02083 | hp1 | a0003 | c0005 | t0001 | g0150 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02145 | hp1 | a0002 | c0004 | t0001 | g0025 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CDX | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02615 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02615 | hp2 | a0003 | c0005 | t0001 | g0149 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0145 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0006 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0140 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02886 | hp2 | a0003 | c0005 | t0001 | g0155 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0023 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0025 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0040 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03225 | hp1 | a0009 | c0010 | t0001 | g0010 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03239 | hp1 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0139 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03490 | hp2 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ESN | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0024 | SAS | PJL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0067 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18522 | hp2 | a0003 | c0005 | t0001 | g0153 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18942 | hp1 | a0003 | c0005 | t0001 | g0168 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18966 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18974 | hp2 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18975 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0138 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18998 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19007 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19043 | hp1 | a0002 | c0004 | t0001 | g0039 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19054 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19057 | hp2 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19068 | hp1 | a0004 | c0006 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19240 | hp1 | a0003 | c0005 | t0001 | g0154 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | YRI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ASW | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0144 | SAS | GIH | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0136 | AFR | ACB | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | MSL | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | USA | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0039 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0172 | REF | REF | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0010 | REF | REF | NUF2_chr1_163316954_163360759 | NUF2 | chr1 | 163316954 | 163360759 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:163328247 | T | C | 1 | a0007 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.218T>C | p.Val73Ala | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/14 | 497/1964 | 218/1395 | 73/464 | chr1 | 163328247 | |||
| chr1:163338056 | G | A | 1 | a0006 | 1 | HG00738.hp2 | missense_variant | MODERATE | c.472G>A | p.Ala158Thr | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/14 | 751/1964 | 472/1395 | 158/464 | chr1 | 163338056 | |||
| chr1:163340421 | C | T | 1 | a0009 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.664C>T | p.Arg222Cys | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/14 | 943/1964 | 664/1395 | 222/464 | chr1 | 163340421 | |||
| chr1:163343749 | C | T | 1 | a0002 | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.686C>T | p.Ser229Leu | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/14 | 965/1964 | 686/1395 | 229/464 | chr1 | 163343749 | |||
| chr1:163343778 | A | C | 1 | a0003 | 8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
missense_variant | MODERATE | c.715A>C | p.Ser239Arg | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/14 | 994/1964 | 715/1395 | 239/464 | chr1 | 163343778 | |||
| chr1:163347798 | G | C | 1 | a0005 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.984G>C | p.Glu328Asp | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/14 | 1263/1964 | 984/1395 | 328/464 | chr1 | 163347798 | |||
| chr1:163348989 | G | A | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1169G>A | p.Arg390Gln | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/14 | 1448/1964 | 1169/1395 | 390/464 | chr1 | 163348989 | |||
| chr1:163355380 | G | A | 1 | a0004 | 6 | NA18966.hp1 NA18975.hp2 NA19007.hp1 others(3): Show |
missense_variant | MODERATE | c.1306G>A | p.Gly436Ser | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 1585/1964 | 1306/1395 | 436/464 | chr1 | 163355380 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:163327532 | A | C | 1 | a0002c0003 | 25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
synonymous_variant | LOW | c.168A>C | p.Val56Val | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/14 | 447/1964 | 168/1395 | 56/464 | chr1 | 163327532 | |||
| chr1:163339429 | A | T | 3 | a0001c0001 a0003c0005 a0008c0011 |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
synonymous_variant | LOW | c.558A>T | p.Gly186Gly | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/14 | 837/1964 | 558/1395 | 186/464 | chr1 | 163339429 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:163321959 | G | A | 1 | a0001c0002t0002 | 2 | HG02683.hp1 HG03654.hp2 |
5_prime_UTR_variant | MODIFIER | c.-274G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/14 | 4093 | chr1 | 163321959 | ||||||
| chr1:163322180 | T | A | 1 | a0001c0002t0003 | 1 | HG00438.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/14 | 3872 | chr1 | 163322180 | ||||||
| chr1:163355665 | G | A | 1 | a0001c0001t0004 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 196 | chr1 | 163355665 | ||||||
| chr1:163355685 | T | C | 1 | a0001c0001t0005 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 14/14 | 216 | chr1 | 163355685 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:163322250 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(65): Show |
116 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-21+38T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322250 | |||||||
| chr1:163322318 | G | T | 1 | a0001c0002t0001g0200 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-21+106G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322318 | |||||||
| chr1:163322427 | T | C | 54 | a0001c0001t0001g0102 a0001c0002t0001g0001 a0001c0002t0001g0002 others(51): Show |
124 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-21+215T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322427 | |||||||
| chr1:163322495 | T | C | 1 | a0001c0002t0001g0099 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-21+283T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322495 | |||||||
| chr1:163322572 | T | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-21+360T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322572 | |||||||
| chr1:163322602 | T | C | 20 | a0001c0002t0001g0146 a0002c0003t0001g0006 a0002c0003t0001g0038 others(17): Show |
41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.-21+390T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322602 | |||||||
| chr1:163322652 | C | A | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-21+440C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322652 | |||||||
| chr1:163322746 | C | T | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+534C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322746 | |||||||
| chr1:163322789 | T | G | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+577T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322789 | |||||||
| chr1:163322874 | A | G | 1 | a0008c0011t0001g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-21+662A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322874 | |||||||
| chr1:163322971 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-21+759G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163322971 | |||||||
| chr1:163323439 | G | A | 7 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(4): Show |
7 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+1227G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323439 | |||||||
| chr1:163323589 | G | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21+1377G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323589 | |||||||
| chr1:163323838 | A | G | 2 | a0003c0005t0001g0154 a0003c0005t0001g0155 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-21+1626A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163323838 | |||||||
| chr1:163323987 | T | TA | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.-21+1776dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163323987 | ||||||
| chr1:163324119 | A | G | 5 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(2): Show |
5 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+1907A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324119 | |||||||
| chr1:163324229 | G | A | 1 | a0001c0002t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20-1803G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324229 | |||||||
| chr1:163324242 | CAG | C | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-1786_-20-1785d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324242 | ||||||
| chr1:163324408 | T | A | 1 | a0001c0002t0001g0101 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-20-1624T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324408 | |||||||
| chr1:163324435 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-20-1597T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324435 | |||||||
| chr1:163324513 | T | TA | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-20-1512dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324513 | ||||||
| chr1:163324544 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-20-1488G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324544 | |||||||
| chr1:163324738 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-20-1294G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324738 | |||||||
| chr1:163324757 | T | G | 2 | a0001c0002t0001g0103 a0008c0011t0001g0177 |
2 | HG01891.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-20-1275T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324757 | |||||||
| chr1:163324838 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
367 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.-20-1194T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324838 | |||||||
| chr1:163324882 | G | GTTTCT | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-20-1137_-20-1133d others(7): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324882 | ||||||
| chr1:163324882 | G | GTTTCTTT others(3): Show |
1 | a0003c0005t0001g0168 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-20-1142_-20-1133d others(12): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324882 | ||||||
| chr1:163324892 | T | TTTTCTTT others(2): Show |
9 | a0001c0001t0001g0035 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
10 | HG01255.hp2 HG01433.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20-1133_-20-1132i others(11): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324892 | ||||||
| chr1:163324896 | C | CT | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1133dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324896 | ||||||
| chr1:163324900 | C | CT | 54 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(51): Show |
132 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.-20-1114dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324900 | ||||||
| chr1:163324900 | C | T | 2 | a0001c0002t0001g0146 a0002c0003t0001g0147 |
2 | HG02258.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-20-1132C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324900 | |||||||
| chr1:163324901 | T | TTTC | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
147 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(5): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324901 | ||||||
| chr1:163324902 | T | TTC | 16 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0046 others(13): Show |
22 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163324902 | ||||||
| chr1:163324903 | T | TC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
9 | HG01069.hp1 HG01070.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20-1129_-20-1128i others(3): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324903 | |||||||
| chr1:163324966 | A | G | 1 | a0001c0002t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-20-1066A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163324966 | |||||||
| chr1:163325087 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-20-945G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325087 | |||||||
| chr1:163325094 | A | G | 14 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(11): Show |
29 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-20-938A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325094 | |||||||
| chr1:163325231 | C | T | 3 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0186 |
3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-20-801C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325231 | |||||||
| chr1:163325276 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0048 |
3 | HG02976.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-756C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325276 | |||||||
| chr1:163325425 | A | C | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(50): Show |
123 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-20-607A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325425 | |||||||
| chr1:163325544 | A | C | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.-20-488A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325544 | |||||||
| chr1:163325608 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-20-424A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325608 | |||||||
| chr1:163325615 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20-417A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325615 | |||||||
| chr1:163325631 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-20-401T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325631 | |||||||
| chr1:163325692 | TG | T | 3 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0186 |
3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-20-338delG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 163325692 | ||||||
| chr1:163325709 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0004g0051 |
3 | HG01069.hp2 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-20-323G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325709 | |||||||
| chr1:163325751 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-281A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325751 | |||||||
| chr1:163325783 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20-249T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325783 | |||||||
| chr1:163325786 | T | G | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-20-246T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325786 | |||||||
| chr1:163325888 | A | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-20-144A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325888 | |||||||
| chr1:163325957 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-20-75C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 1/13 | chr1 | 163325957 | |||||||
| chr1:163326208 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.123+34G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326208 | |||||||
| chr1:163326267 | C | T | 1 | a0001c0001t0001g0033 | 2 | NA18982.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.123+93C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326267 | |||||||
| chr1:163326282 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.123+108C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326282 | |||||||
| chr1:163326303 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.123+129G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326303 | |||||||
| chr1:163326404 | T | TA | 32 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(29): Show |
65 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.123+242dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | ||||||
| chr1:163326404 | T | TAA | 59 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(56): Show |
107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.123+241_123+242dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | ||||||
| chr1:163326404 | T | TAAA | 12 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0057 others(9): Show |
12 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+240_123+242dup others(3): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | ||||||
| chr1:163326404 | TA | T | 15 | a0001c0002t0001g0134 a0002c0003t0001g0006 a0002c0003t0001g0038 others(12): Show |
30 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.123+242delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163326404 | ||||||
| chr1:163326503 | C | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.123+329C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326503 | |||||||
| chr1:163326950 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.124-538C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163326950 | |||||||
| chr1:163327098 | T | TCA | 3 | a0001c0002t0001g0188 a0001c0002t0001g0189 a0001c0002t0001g0190 |
3 | HG01952.hp1 HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.124-347_124-346dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | T | TCTTTAAA others(3): Show |
1 | a0001c0002t0001g0132 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.124-389_124-388ins others(10): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | T | TCTTTAAA others(5): Show |
1 | a0001c0002t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.124-389_124-388ins others(12): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCA | T | 5 | a0001c0002t0001g0044 a0001c0002t0001g0133 a0001c0002t0001g0146 others(2): Show |
6 | HG01433.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-347_124-346del others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCACA | T | 2 | a0001c0002t0001g0041 a0003c0005t0001g0168 |
3 | HG02895.hp2 HG02897.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.124-349_124-346del others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCACACA | T | 12 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0001c0002t0001g0184 others(9): Show |
12 | HG00423.hp1 HG01175.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-351_124-346del others(6): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCACACAC others(1): Show |
T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(6): Show |
19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.124-353_124-346del others(8): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCACACAC others(7): Show |
T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-359_124-346del others(14): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327098 | TCACACAC others(9): Show |
T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-361_124-346del others(16): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327098 | ||||||
| chr1:163327099 | C | CTT | 45 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(42): Show |
105 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | |||||||
| chr1:163327099 | C | CTTTA | 10 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0009 others(7): Show |
12 | HG00673.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | |||||||
| chr1:163327099 | C | CTTTAAA | 5 | a0001c0002t0001g0001 a0001c0002t0001g0013 a0001c0002t0001g0042 others(2): Show |
10 | HG01109.hp2 HG02165.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-389_124-388ins others(6): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327099 | |||||||
| chr1:163327100 | A | T | 47 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(44): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.124-388A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327100 | |||||||
| chr1:163327101 | C | A | 51 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(48): Show |
118 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.124-387C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327101 | |||||||
| chr1:163327101 | C | T | 5 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0021 others(2): Show |
6 | HG01169.hp2 HG01981.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-387C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327101 | |||||||
| chr1:163327102 | A | T | 6 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0021 others(3): Show |
7 | HG01169.hp2 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-386A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327102 | |||||||
| chr1:163327103 | C | A | 47 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(44): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.124-385C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327103 | |||||||
| chr1:163327103 | C | T | 2 | a0001c0002t0001g0133 a0001c0002t0001g0146 |
2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.124-385C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327103 | |||||||
| chr1:163327104 | A | T | 3 | a0001c0002t0001g0133 a0001c0002t0001g0146 a0003c0005t0001g0168 |
3 | HG01433.hp1 HG02258.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.124-384A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327104 | |||||||
| chr1:163327105 | C | A | 6 | a0001c0002t0001g0002 a0001c0002t0001g0018 a0001c0002t0001g0021 others(3): Show |
7 | HG01169.hp2 HG01433.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-383C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327105 | |||||||
| chr1:163327105 | C | T | 1 | a0003c0005t0001g0168 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.124-383C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327105 | |||||||
| chr1:163327106 | A | T | 10 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0003c0005t0001g0149 others(7): Show |
10 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-382A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327106 | |||||||
| chr1:163327107 | C | A | 3 | a0001c0002t0001g0133 a0001c0002t0001g0146 a0003c0005t0001g0168 |
3 | HG01433.hp1 HG02258.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.124-381C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327107 | |||||||
| chr1:163327107 | C | T | 9 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0003c0005t0001g0149 others(6): Show |
9 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-381C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327107 | |||||||
| chr1:163327108 | A | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(15): Show |
28 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.124-380A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327108 | |||||||
| chr1:163327109 | C | A | 10 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0003c0005t0001g0149 others(7): Show |
10 | HG00423.hp1 HG01175.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.124-379C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327109 | |||||||
| chr1:163327109 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(6): Show |
19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.124-379C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327109 | |||||||
| chr1:163327110 | A | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(6): Show |
19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.124-378A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327110 | |||||||
| chr1:163327111 | C | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(15): Show |
28 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.124-377C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327111 | |||||||
| chr1:163327113 | C | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(6): Show |
19 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.124-375C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327113 | |||||||
| chr1:163327114 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-374A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327114 | |||||||
| chr1:163327115 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-373C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327115 | |||||||
| chr1:163327116 | A | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.124-372A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327116 | |||||||
| chr1:163327117 | C | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.124-371C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327117 | |||||||
| chr1:163327117 | C | T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-371C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327117 | |||||||
| chr1:163327118 | A | T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-370A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327118 | |||||||
| chr1:163327119 | C | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.124-369C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327119 | |||||||
| chr1:163327121 | C | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.124-367C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327121 | |||||||
| chr1:163327130 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.124-358A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327130 | |||||||
| chr1:163327139 | C | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0131 a0001c0002t0001g0135 |
4 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-349C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327139 | |||||||
| chr1:163327193 | G | T | 1 | a0001c0002t0001g0186 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.124-295G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327193 | |||||||
| chr1:163327211 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.124-277T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327211 | |||||||
| chr1:163327218 | TA | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0085 |
9 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-268delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 163327218 | ||||||
| chr1:163327228 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.124-260G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327228 | |||||||
| chr1:163327240 | T | C | 12 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(9): Show |
25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-248T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 2/13 | chr1 | 163327240 | |||||||
| chr1:163327591 | G | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.198+29G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327591 | |||||||
| chr1:163327760 | A | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.198+198A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327760 | |||||||
| chr1:163327808 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.198+246T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327808 | |||||||
| chr1:163327828 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+266T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327828 | |||||||
| chr1:163327956 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.199-272G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327956 | |||||||
| chr1:163327994 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-234A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163327994 | |||||||
| chr1:163328029 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0082 |
3 | HG02056.hp2 HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.199-199A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328029 | |||||||
| chr1:163328106 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.199-122G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328106 | |||||||
| chr1:163328119 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0059 others(3): Show |
9 | HG01123.hp1 HG01255.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-109G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 3/13 | chr1 | 163328119 | |||||||
| chr1:163328587 | T | G | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-259T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/13 | chr1 | 163328587 | |||||||
| chr1:163328758 | T | C | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.276-88T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 4/13 | chr1 | 163328758 | |||||||
| chr1:163328946 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337+39G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163328946 | |||||||
| chr1:163328978 | T | TA | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.337+86dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163328978 | ||||||
| chr1:163329041 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.337+134T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329041 | |||||||
| chr1:163329179 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.337+272A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329179 | |||||||
| chr1:163329243 | A | G | 1 | a0001c0002t0001g0130 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.337+336A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329243 | |||||||
| chr1:163329277 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+370A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329277 | |||||||
| chr1:163329325 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.337+418T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329325 | |||||||
| chr1:163329465 | G | T | 1 | a0001c0002t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.337+558G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329465 | |||||||
| chr1:163329788 | T | C | 3 | a0001c0002t0001g0007 a0001c0002t0001g0109 a0004c0006t0001g0007 |
11 | HG00621.hp1 NA18943.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.337+881T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329788 | |||||||
| chr1:163329790 | C | G | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.337+883C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329790 | |||||||
| chr1:163329791 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+884A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329791 | |||||||
| chr1:163329857 | G | A | 2 | a0002c0003t0001g0038 a0002c0003t0001g0138 |
3 | NA18957.hp2 NA18987.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.337+950G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329857 | |||||||
| chr1:163329868 | C | T | 1 | a0001c0002t0001g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.337+961C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329868 | |||||||
| chr1:163329900 | G | A | 5 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(2): Show |
5 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+993G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163329900 | |||||||
| chr1:163330086 | A | G | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1179A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330086 | |||||||
| chr1:163330375 | T | G | 2 | a0001c0002t0001g0104 a0001c0002t0001g0110 |
2 | HG00544.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.337+1468T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330375 | |||||||
| chr1:163330429 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.337+1522G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330429 | |||||||
| chr1:163330499 | C | G | 1 | a0001c0002t0001g0129 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.337+1592C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330499 | |||||||
| chr1:163330693 | C | T | 1 | a0002c0003t0001g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.337+1786C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330693 | |||||||
| chr1:163330726 | C | A | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+1819C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330726 | |||||||
| chr1:163330870 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.337+1963A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163330870 | |||||||
| chr1:163330928 | A | AT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(79): Show |
147 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.337+2032dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163330928 | ||||||
| chr1:163330928 | A | ATT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(20): Show |
39 | HG00099.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.337+2031_337+2032d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163330928 | ||||||
| chr1:163331025 | C | CT | 5 | a0001c0002t0001g0037 a0001c0002t0001g0109 a0001c0002t0001g0128 others(2): Show |
6 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+2134dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | ||||||
| chr1:163331025 | CT | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(32): Show |
66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.337+2134delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | ||||||
| chr1:163331025 | CTT | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.337+2133_337+2134d others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163331025 | ||||||
| chr1:163331079 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.337+2172G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331079 | |||||||
| chr1:163331161 | G | A | 3 | a0001c0001t0001g0180 a0001c0002t0001g0111 a0001c0002t0001g0128 |
3 | HG02622.hp2 HG03834.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.337+2254G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331161 | |||||||
| chr1:163331195 | A | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.337+2288A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331195 | |||||||
| chr1:163331257 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.337+2350C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331257 | |||||||
| chr1:163331258 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.337+2351G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331258 | |||||||
| chr1:163331277 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.337+2370A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331277 | |||||||
| chr1:163331306 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.337+2399T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331306 | |||||||
| chr1:163331537 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.337+2630C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331537 | |||||||
| chr1:163331594 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.337+2687T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331594 | |||||||
| chr1:163331943 | T | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(66): Show |
117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.337+3036T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331943 | |||||||
| chr1:163331947 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.337+3040G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163331947 | |||||||
| chr1:163332092 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0167 |
2 | NA18973.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.337+3185T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332092 | |||||||
| chr1:163332229 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.337+3322C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332229 | |||||||
| chr1:163332278 | G | A | 1 | a0001c0002t0001g0021 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337+3371G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332278 | |||||||
| chr1:163332480 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.337+3573G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332480 | |||||||
| chr1:163332494 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.337+3587C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332494 | |||||||
| chr1:163332675 | C | G | 1 | a0002c0003t0001g0144 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.337+3768C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332675 | |||||||
| chr1:163332703 | C | T | 3 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0186 |
3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.337+3796C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332703 | |||||||
| chr1:163332937 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.338-3814T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332937 | |||||||
| chr1:163332999 | T | C | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(50): Show |
123 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.338-3752T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163332999 | |||||||
| chr1:163333021 | A | G | 1 | a0003c0005t0001g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.338-3730A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333021 | |||||||
| chr1:163333245 | G | T | 1 | a0001c0002t0001g0036 | 2 | HG02135.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.338-3506G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333245 | |||||||
| chr1:163333309 | G | A | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.338-3442G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333309 | |||||||
| chr1:163333322 | A | G | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-3429A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333322 | |||||||
| chr1:163333323 | C | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-3428C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333323 | |||||||
| chr1:163333397 | T | C | 1 | a0001c0002t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.338-3354T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333397 | |||||||
| chr1:163333513 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.338-3238T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333513 | |||||||
| chr1:163333798 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.338-2953A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333798 | |||||||
| chr1:163333867 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.338-2884C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163333867 | |||||||
| chr1:163334035 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.338-2716A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334035 | |||||||
| chr1:163334039 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.338-2712A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334039 | |||||||
| chr1:163334226 | C | T | 3 | a0003c0005t0001g0150 a0003c0005t0001g0151 a0003c0005t0001g0152 |
3 | HG00423.hp1 HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.338-2525C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334226 | |||||||
| chr1:163334227 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.338-2524G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334227 | |||||||
| chr1:163334537 | A | G | 1 | a0002c0004t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.338-2214A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334537 | |||||||
| chr1:163334568 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-2183G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334568 | |||||||
| chr1:163334684 | G | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.338-2067G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334684 | |||||||
| chr1:163334685 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.338-2066G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334685 | |||||||
| chr1:163334754 | G | A | 3 | a0002c0004t0001g0024 a0002c0004t0001g0039 a0002c0004t0001g0148 |
6 | HG02004.hp1 HG03239.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-1997G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334754 | |||||||
| chr1:163334820 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.338-1931T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334820 | |||||||
| chr1:163334843 | A | G | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-1908A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334843 | |||||||
| chr1:163334903 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.338-1848A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334903 | |||||||
| chr1:163334951 | TG | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(8): Show |
21 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.338-1799delG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163334951 | |||||||
| chr1:163334952 | G | GT | 6 | a0001c0001t0001g0092 a0002c0004t0001g0024 a0002c0004t0001g0025 others(3): Show |
12 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.338-1791dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163334952 | ||||||
| chr1:163335027 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-1724T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335027 | |||||||
| chr1:163335203 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-1548C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335203 | |||||||
| chr1:163335217 | G | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.338-1534G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335217 | |||||||
| chr1:163335414 | G | T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-1337G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335414 | |||||||
| chr1:163335461 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.338-1290T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335461 | |||||||
| chr1:163335555 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-1196T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335555 | |||||||
| chr1:163335565 | G | GT | 3 | a0001c0001t0001g0092 a0001c0001t0001g0180 a0001c0002t0001g0018 |
6 | HG00438.hp2 HG02622.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-1177dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163335565 | ||||||
| chr1:163335604 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.338-1147C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335604 | |||||||
| chr1:163335634 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-1117T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335634 | |||||||
| chr1:163335640 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-1111T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335640 | |||||||
| chr1:163335893 | A | G | 2 | a0001c0002t0001g0127 a0001c0002t0001g0129 |
2 | NA18985.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.338-858A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335893 | |||||||
| chr1:163335938 | T | A | 1 | a0001c0002t0001g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.338-813T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163335938 | |||||||
| chr1:163336045 | A | G | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-706A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336045 | |||||||
| chr1:163336075 | CT | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(15): Show |
28 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.338-675delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336075 | |||||||
| chr1:163336169 | CT | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-580delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 163336169 | ||||||
| chr1:163336316 | C | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-435C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336316 | |||||||
| chr1:163336387 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.338-364G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336387 | |||||||
| chr1:163336446 | T | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.338-305T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336446 | |||||||
| chr1:163336580 | C | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.338-171C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336580 | |||||||
| chr1:163336580 | C | T | 1 | a0001c0002t0001g0126 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.338-171C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336580 | |||||||
| chr1:163336606 | G | A | 1 | a0003c0005t0001g0154 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.338-145G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336606 | |||||||
| chr1:163336641 | G | T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.338-110G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336641 | |||||||
| chr1:163336733 | T | G | 8 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(5): Show |
8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.338-18T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 5/13 | chr1 | 163336733 | |||||||
| chr1:163337055 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.435+207C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337055 | |||||||
| chr1:163337200 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.435+352A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337200 | |||||||
| chr1:163337346 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.435+498C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337346 | |||||||
| chr1:163337362 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.435+514G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337362 | |||||||
| chr1:163337483 | G | A | 1 | a0001c0002t0001g0027 | 3 | HG02258.hp2 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.436-537G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337483 | |||||||
| chr1:163337509 | C | T | 7 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(4): Show |
7 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-511C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337509 | |||||||
| chr1:163337638 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.436-382A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337638 | |||||||
| chr1:163337684 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.436-336A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337684 | |||||||
| chr1:163337697 | G | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02486.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.436-323G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337697 | |||||||
| chr1:163337964 | A | G | 3 | a0001c0002t0001g0037 a0001c0002t0001g0131 a0001c0002t0001g0135 |
4 | HG01081.hp2 HG01123.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-56A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 6/13 | chr1 | 163337964 | |||||||
| chr1:163338154 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.509+61T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338154 | |||||||
| chr1:163338237 | T | TA | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(32): Show |
61 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.509+158dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | ||||||
| chr1:163338237 | T | TAA | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
148 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.509+157_509+158dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | ||||||
| chr1:163338237 | TA | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.509+158delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338237 | ||||||
| chr1:163338466 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.509+373A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338466 | |||||||
| chr1:163338854 | A | G | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-527A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163338854 | |||||||
| chr1:163338933 | CAGAT | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.510-445_510-442del others(4): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 163338933 | ||||||
| chr1:163339029 | G | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(66): Show |
117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.510-352G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339029 | |||||||
| chr1:163339036 | AGTAAGAG others(3): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.510-344_510-335del others(10): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339036 | |||||||
| chr1:163339318 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0087 |
4 | HG00408.hp2 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-63G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339318 | |||||||
| chr1:163339319 | G | T | 3 | a0001c0002t0001g0028 a0001c0002t0001g0190 a0001c0002t0001g0199 |
5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-62G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 7/13 | chr1 | 163339319 | |||||||
| chr1:163339484 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
splice_region_variant&intron_variant | LOW | c.606+7G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339484 | |||||||
| chr1:163339512 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.606+35C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339512 | |||||||
| chr1:163339655 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.606+178G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339655 | |||||||
| chr1:163339779 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.606+302C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339779 | |||||||
| chr1:163339843 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.606+366T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339843 | |||||||
| chr1:163339902 | T | C | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.606+425T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339902 | |||||||
| chr1:163339907 | G | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.606+430G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163339907 | |||||||
| chr1:163340016 | C | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.607-348C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340016 | |||||||
| chr1:163340039 | C | T | 1 | a0002c0004t0001g0040 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.607-325C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340039 | |||||||
| chr1:163340106 | T | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.607-258T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340106 | |||||||
| chr1:163340230 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.607-134G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 8/13 | chr1 | 163340230 | |||||||
| chr1:163340469 | A | G | 2 | a0001c0002t0001g0101 a0001c0002t0001g0124 |
2 | HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.669+43A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340469 | |||||||
| chr1:163340508 | G | GTTTGTGG others(10): Show |
1 | a0001c0002t0002g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+82_669+83insTT others(15): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340508 | |||||||
| chr1:163340509 | G | T | 1 | a0001c0002t0002g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+83G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340509 | |||||||
| chr1:163340510 | C | A | 1 | a0001c0002t0002g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+84C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340510 | |||||||
| chr1:163340511 | A | T | 1 | a0001c0002t0002g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.669+85A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340511 | |||||||
| chr1:163340720 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.669+294T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340720 | |||||||
| chr1:163340761 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+335G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340761 | |||||||
| chr1:163340799 | A | C | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+373A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340799 | |||||||
| chr1:163340921 | A | G | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669+495A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340921 | |||||||
| chr1:163340942 | A | G | 7 | a0001c0002t0001g0002 a0001c0002t0001g0022 a0001c0002t0001g0036 others(4): Show |
26 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.669+516A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163340942 | |||||||
| chr1:163341030 | A | C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0190 a0001c0002t0001g0199 |
5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+604A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341030 | |||||||
| chr1:163341036 | A | G | 1 | a0001c0002t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.669+610A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341036 | |||||||
| chr1:163341139 | A | C | 1 | a0001c0002t0001g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.669+713A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341139 | |||||||
| chr1:163341178 | G | GA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0050 a0001c0001t0001g0052 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.669+761dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 163341178 | ||||||
| chr1:163341204 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.669+778C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341204 | |||||||
| chr1:163341213 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0065 |
2 | NA18947.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.669+787T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341213 | |||||||
| chr1:163341297 | C | T | 1 | a0003c0005t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.669+871C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341297 | |||||||
| chr1:163341309 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.669+883G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341309 | |||||||
| chr1:163341399 | G | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(21): Show |
49 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.669+973G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341399 | |||||||
| chr1:163341416 | T | C | 1 | a0002c0003t0001g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.669+990T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341416 | |||||||
| chr1:163341455 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0088 |
2 | HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.669+1029G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341455 | |||||||
| chr1:163341460 | G | A | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.669+1034G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341460 | |||||||
| chr1:163341493 | C | T | 2 | a0001c0002t0001g0189 a0001c0002t0001g0193 |
2 | HG01358.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.669+1067C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341493 | |||||||
| chr1:163341641 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
12 | HG02074.hp2 HG03927.hp1 HG04199.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+1215T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341641 | |||||||
| chr1:163341881 | C | T | 13 | a0001c0002t0001g0007 a0001c0002t0001g0009 a0001c0002t0001g0018 others(10): Show |
33 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.669+1455C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341881 | |||||||
| chr1:163341927 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.669+1501G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163341927 | |||||||
| chr1:163342057 | G | A | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+1631G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342057 | |||||||
| chr1:163342220 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670-1513C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342220 | |||||||
| chr1:163342436 | A | G | 1 | a0002c0004t0001g0025 | 3 | HG01243.hp2 HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.670-1297A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342436 | |||||||
| chr1:163342494 | A | C | 1 | a0001c0002t0001g0112 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.670-1239A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342494 | |||||||
| chr1:163342597 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
156 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.670-1136A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342597 | |||||||
| chr1:163342627 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.670-1106T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342627 | |||||||
| chr1:163342711 | T | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.670-1022T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342711 | |||||||
| chr1:163342762 | C | A | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-971C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342762 | |||||||
| chr1:163342827 | G | A | 1 | a0001c0002t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.670-906G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163342827 | |||||||
| chr1:163343109 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.670-624A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343109 | |||||||
| chr1:163343112 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.670-621C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343112 | |||||||
| chr1:163343167 | G | C | 12 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(9): Show |
25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.670-566G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343167 | |||||||
| chr1:163343186 | G | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.670-547G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343186 | |||||||
| chr1:163343258 | A | G | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.670-475A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343258 | |||||||
| chr1:163343400 | C | A | 1 | a0003c0005t0001g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.670-333C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343400 | |||||||
| chr1:163343472 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.670-261G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343472 | |||||||
| chr1:163343528 | G | C | 1 | a0003c0005t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.670-205G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 9/13 | chr1 | 163343528 | |||||||
| chr1:163344020 | T | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
156 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.807+150T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344020 | |||||||
| chr1:163344042 | A | C | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.807+172A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344042 | |||||||
| chr1:163344080 | A | G | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.807+210A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344080 | |||||||
| chr1:163344090 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(15): Show |
28 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.807+220G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344090 | |||||||
| chr1:163344129 | G | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.807+259G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344129 | |||||||
| chr1:163344265 | T | G | 1 | a0001c0001t0001g0066 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.807+395T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344265 | |||||||
| chr1:163344453 | C | T | 1 | a0002c0003t0001g0142 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.807+583C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344453 | |||||||
| chr1:163344460 | T | TAA | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.807+598_807+599dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344460 | ||||||
| chr1:163344472 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.807+602C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344472 | |||||||
| chr1:163344571 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.807+701G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344571 | |||||||
| chr1:163344641 | T | TAGAAGTG others(325): Show |
14 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0035 others(11): Show |
18 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(324): Show |
1 | a0001c0001t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(322): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0087 |
3 | HG00639.hp2 NA18954.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.807+783_807+784ins others(329): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(323): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0032 others(19): Show |
37 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(330): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(324): Show |
10 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0075 others(7): Show |
10 | HG01070.hp1 HG01433.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(325): Show |
22 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(19): Show |
54 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(326): Show |
5 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG01928.hp1 HG02486.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(333): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(324): Show |
1 | a0001c0001t0001g0060 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(325): Show |
14 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
33 | HG00408.hp1 HG00621.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(323): Show |
1 | a0001c0001t0001g0031 | 2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.807+783_807+784ins others(330): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(324): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(5): Show |
18 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.807+783_807+784ins others(331): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344641 | T | TAGAAGTG others(325): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG01175.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.807+783_807+784ins others(332): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 163344641 | ||||||
| chr1:163344720 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.807+850G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163344720 | |||||||
| chr1:163345139 | A | G | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.808-539A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345139 | |||||||
| chr1:163345263 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0156 a0001c0001t0001g0158 others(2): Show |
12 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.808-415G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345263 | |||||||
| chr1:163345296 | G | A | 3 | a0001c0002t0001g0028 a0001c0002t0001g0190 a0001c0002t0001g0199 |
5 | HG02055.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.808-382G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345296 | |||||||
| chr1:163345329 | A | G | 1 | a0001c0002t0001g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.808-349A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345329 | |||||||
| chr1:163345371 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.808-307T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345371 | |||||||
| chr1:163345395 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.808-283T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345395 | |||||||
| chr1:163345540 | C | T | 2 | a0002c0004t0001g0024 a0002c0004t0001g0148 |
4 | HG02004.hp1 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.808-138C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345540 | |||||||
| chr1:163345560 | G | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.808-118G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 10/13 | chr1 | 163345560 | |||||||
| chr1:163345932 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0056 others(4): Show |
10 | HG02074.hp2 NA18941.hp2 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.948+114C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163345932 | |||||||
| chr1:163346068 | A | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(7): Show |
20 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.948+250A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346068 | |||||||
| chr1:163346082 | G | A | 2 | a0001c0002t0001g0191 a0001c0002t0001g0195 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.948+264G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346082 | |||||||
| chr1:163346101 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.948+283A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346101 | |||||||
| chr1:163346123 | G | A | 3 | a0001c0002t0001g0184 a0001c0002t0001g0185 a0001c0002t0001g0186 |
3 | HG02055.hp2 HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.948+305G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346123 | |||||||
| chr1:163346251 | TA | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.948+437delA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 163346251 | ||||||
| chr1:163346322 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.948+504T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346322 | |||||||
| chr1:163346474 | G | A | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.948+656G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346474 | |||||||
| chr1:163346561 | T | G | 1 | a0003c0005t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.948+743T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346561 | |||||||
| chr1:163346625 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
183 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.948+807C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346625 | |||||||
| chr1:163346678 | A | G | 8 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(5): Show |
8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.948+860A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346678 | |||||||
| chr1:163346716 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.948+898A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163346716 | |||||||
| chr1:163346851 | G | GCA | 15 | a0001c0001t0001g0064 a0002c0003t0001g0006 a0002c0003t0001g0038 others(12): Show |
30 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.949-897_949-896dup others(2): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 163346851 | ||||||
| chr1:163347003 | G | T | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-760G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347003 | |||||||
| chr1:163347016 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.949-747T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347016 | |||||||
| chr1:163347178 | G | A | 1 | a0001c0002t0001g0037 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.949-585G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347178 | |||||||
| chr1:163347264 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.949-499G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347264 | |||||||
| chr1:163347392 | C | G | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.949-371C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347392 | |||||||
| chr1:163347532 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.949-231A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347532 | |||||||
| chr1:163347544 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.949-219C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347544 | |||||||
| chr1:163347626 | G | A | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.949-137G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347626 | |||||||
| chr1:163347637 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.949-126T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 11/13 | chr1 | 163347637 | |||||||
| chr1:163348000 | TC | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1124+67delC | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 163348000 | ||||||
| chr1:163348021 | C | T | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1124+83C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348021 | |||||||
| chr1:163348030 | C | T | 1 | a0001c0002t0001g0021 | 3 | HG01168.hp2 HG01169.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1124+92C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348030 | |||||||
| chr1:163348214 | A | T | 2 | a0001c0002t0001g0178 a0001c0002t0001g0179 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1124+276A>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348214 | |||||||
| chr1:163348349 | T | G | 3 | a0001c0002t0001g0189 a0001c0002t0001g0192 a0001c0002t0001g0193 |
3 | HG01358.hp1 HG01952.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1124+411T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348349 | |||||||
| chr1:163348439 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1124+501C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348439 | |||||||
| chr1:163348487 | G | A | 1 | a0008c0011t0001g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1125-458G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348487 | |||||||
| chr1:163348543 | C | A | 1 | a0001c0002t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1125-402C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348543 | |||||||
| chr1:163348719 | G | GA | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1125-218dupA | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 163348719 | ||||||
| chr1:163348927 | G | C | 1 | a0001c0002t0001g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1125-18G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 12/13 | chr1 | 163348927 | |||||||
| chr1:163349088 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA18979.hp1 | splice_region_variant&intron_variant | LOW | c.1260+8T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349088 | |||||||
| chr1:163349144 | A | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1260+64A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349144 | |||||||
| chr1:163349272 | C | T | 2 | a0003c0005t0001g0154 a0003c0005t0001g0155 |
2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1260+192C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349272 | |||||||
| chr1:163349325 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1260+245A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349325 | |||||||
| chr1:163349375 | A | C | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1260+295A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349375 | |||||||
| chr1:163349382 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02486.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1260+302A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349382 | |||||||
| chr1:163349435 | G | C | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1260+355G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349435 | |||||||
| chr1:163349449 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1260+369A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349449 | |||||||
| chr1:163349468 | A | G | 1 | a0008c0011t0001g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1260+388A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349468 | |||||||
| chr1:163349564 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1260+484T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349564 | |||||||
| chr1:163349578 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1260+498T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349578 | |||||||
| chr1:163349593 | C | T | 1 | a0008c0011t0001g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1260+513C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349593 | |||||||
| chr1:163349639 | G | A | 1 | a0001c0002t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1260+559G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349639 | |||||||
| chr1:163349712 | A | G | 13 | a0001c0001t0001g0064 a0002c0003t0001g0006 a0002c0003t0001g0038 others(10): Show |
26 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.1260+632A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349712 | |||||||
| chr1:163349762 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+682C>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349762 | |||||||
| chr1:163349799 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+719A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349799 | |||||||
| chr1:163349818 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1260+738G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349818 | |||||||
| chr1:163349911 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0048 |
3 | HG02976.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1260+831T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163349911 | |||||||
| chr1:163350076 | C | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0007 others(56): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1260+996C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350076 | |||||||
| chr1:163350159 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.1260+1079A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350159 | |||||||
| chr1:163350162 | C | T | 1 | a0001c0002t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1260+1082C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350162 | |||||||
| chr1:163350194 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1260+1114C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350194 | |||||||
| chr1:163350219 | G | A | 1 | a0003c0005t0001g0149 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1260+1139G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350219 | |||||||
| chr1:163350227 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1260+1147G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350227 | |||||||
| chr1:163350409 | CAGTTACT others(15): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1260+1340_1260+136 others(26): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163350409 | ||||||
| chr1:163350461 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1260+1381G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350461 | |||||||
| chr1:163350503 | T | C | 2 | a0002c0004t0001g0023 a0002c0004t0001g0136 |
4 | HG01884.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+1423T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350503 | |||||||
| chr1:163350627 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1260+1547T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350627 | |||||||
| chr1:163350733 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0175 |
4 | HG00280.hp1 HG00323.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+1653C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350733 | |||||||
| chr1:163350773 | A | G | 15 | a0001c0001t0001g0064 a0002c0003t0001g0006 a0002c0003t0001g0038 others(12): Show |
30 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.1260+1693A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350773 | |||||||
| chr1:163350778 | A | AT | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1260+1699dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163350778 | ||||||
| chr1:163350790 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0086 |
5 | HG00621.hp2 NA18946.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+1710A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163350790 | |||||||
| chr1:163351067 | A | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(66): Show |
117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1260+1987A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351067 | |||||||
| chr1:163351070 | C | T | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1260+1990C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351070 | |||||||
| chr1:163351337 | A | ATAAAGTT others(19): Show |
1 | a0001c0002t0001g0109 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1260+2259_1260+228 others(30): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163351337 | ||||||
| chr1:163351410 | T | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1260+2330T>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351410 | |||||||
| chr1:163351433 | C | G | 1 | a0001c0002t0001g0041 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1260+2353C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351433 | |||||||
| chr1:163351577 | T | G | 1 | a0002c0004t0001g0040 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1260+2497T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351577 | |||||||
| chr1:163351577 | T | TGCTGCAT others(4): Show |
1 | a0001c0001t0001g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1260+2498_1260+250 others(15): Show |
NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163351577 | ||||||
| chr1:163351608 | G | A | 1 | a0001c0002t0001g0042 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1260+2528G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351608 | |||||||
| chr1:163351630 | T | G | 1 | a0002c0003t0001g0143 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1260+2550T>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351630 | |||||||
| chr1:163351684 | C | T | 21 | a0001c0002t0001g0104 a0001c0002t0001g0110 a0002c0003t0001g0006 others(18): Show |
42 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1260+2604C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351684 | |||||||
| chr1:163351879 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1260+2799A>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351879 | |||||||
| chr1:163351904 | C | G | 2 | a0001c0002t0001g0008 a0001c0002t0001g0106 |
11 | HG00642.hp2 HG01361.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+2824C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163351904 | |||||||
| chr1:163352093 | AT | A | 12 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(9): Show |
25 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260+3016delT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163352093 | ||||||
| chr1:163352243 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-3092A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352243 | |||||||
| chr1:163352272 | C | G | 19 | a0002c0003t0001g0006 a0002c0003t0001g0038 a0002c0003t0001g0137 others(16): Show |
40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1261-3063C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352272 | |||||||
| chr1:163352433 | A | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1261-2902A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352433 | |||||||
| chr1:163352604 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1261-2731C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352604 | |||||||
| chr1:163352662 | C | T | 1 | a0002c0004t0001g0148 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1261-2673C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352662 | |||||||
| chr1:163352737 | G | A | 1 | a0001c0002t0001g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1261-2598G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352737 | |||||||
| chr1:163352758 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1261-2577C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352758 | |||||||
| chr1:163352759 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1261-2576A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352759 | |||||||
| chr1:163352791 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-2544G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352791 | |||||||
| chr1:163352853 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1261-2482G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352853 | |||||||
| chr1:163352881 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-2454A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163352881 | |||||||
| chr1:163353146 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-2189A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353146 | |||||||
| chr1:163353215 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0003g0022 a0002c0003t0001g0140 |
4 | HG00438.hp1 HG02723.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-2120G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353215 | |||||||
| chr1:163353236 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1261-2099A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353236 | |||||||
| chr1:163353259 | T | TG | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1261-2074dupG | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163353259 | ||||||
| chr1:163353425 | G | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1261-1910G>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353425 | |||||||
| chr1:163353490 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(119): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1261-1845G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353490 | |||||||
| chr1:163353506 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1261-1829T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353506 | |||||||
| chr1:163353546 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1261-1789C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353546 | |||||||
| chr1:163353568 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-1767G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353568 | |||||||
| chr1:163353600 | T | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0183 |
3 | HG01891.hp1 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1261-1735T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353600 | |||||||
| chr1:163353622 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1261-1713G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353622 | |||||||
| chr1:163353729 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1261-1606C>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353729 | |||||||
| chr1:163353787 | G | A | 6 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(3): Show |
6 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.1261-1548G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353787 | |||||||
| chr1:163353893 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1261-1442G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163353893 | |||||||
| chr1:163354005 | C | T | 3 | a0002c0003t0001g0038 a0002c0003t0001g0138 a0002c0003t0001g0141 |
4 | NA18957.hp2 NA18974.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-1330C>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354005 | |||||||
| chr1:163354092 | G | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
37 | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1261-1243G>T | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354092 | |||||||
| chr1:163354414 | T | C | 1 | a0001c0002t0001g0120 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1261-921T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354414 | |||||||
| chr1:163354558 | A | G | 5 | a0002c0004t0001g0024 a0002c0004t0001g0025 a0002c0004t0001g0039 others(2): Show |
11 | HG01243.hp2 HG02004.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1261-777A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354558 | |||||||
| chr1:163354668 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(180): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.1261-667G>A | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354668 | |||||||
| chr1:163354687 | A | G | 8 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(5): Show |
8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-648A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354687 | |||||||
| chr1:163354717 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
184 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1261-618A>G | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354717 | |||||||
| chr1:163354778 | T | C | 8 | a0003c0005t0001g0149 a0003c0005t0001g0150 a0003c0005t0001g0151 others(5): Show |
8 | HG00423.hp1 HG02080.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-557T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354778 | |||||||
| chr1:163354827 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1261-508T>C | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | chr1 | 163354827 | |||||||
| chr1:163355139 | C | CT | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.1261-191dupT | NUF2 | ENSG00000143228.13 | transcript | ENST00000271452.8 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 163355139 |