Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129401 |
| ensemblid | ENSG00000163002.13 |
| hgncid | 29797 |
| symbol | NUP35 |
| name | nucleoporin 35 |
| refseq_nuc | NM_138285.5 |
| refseq_prot | NP_612142.2 |
| ensembl_nuc | ENST00000295119.9 |
| ensembl_prot | ENSP00000295119.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 183124443 |
| end | 183161680 |
| strand | + |
| ver | v1.2 |
| region | chr2:183124443-183161680 |
| region5000 | chr2:183119443-183166680 |
| regionname0 | NUP35_chr2_183124443_183161680 |
| regionname5000 | NUP35_chr2_183119443_183166680 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 326 | 401 | 87 | 62 | 192 | 18 | 40 | 146 | NUP35_chr2_183119443_183166680 | NUP35 | MAAFA others(321): Show |
chr2 | 183119443 | 183166680 |
| a0002 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | MAAFA others(321): Show |
chr2 | 183119443 | 183166680 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 978 | 395 | 82 | 62 | 192 | 18 | 39 | NUP35_chr2_183119443_183166680 | NUP35 | ATGGC others(973): Show |
chr2 | 183119443 | 183166680 | ||
| a0001c0002 | 0/0 | 978 | 4 | 4 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | ATGGC others(973): Show |
chr2 | 183119443 | 183166680 | ||
| a0001c0003 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | ATGGC others(973): Show |
chr2 | 183119443 | 183166680 | ||
| a0001c0004 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | ATGGC others(973): Show |
chr2 | 183119443 | 183166680 | ||
| a0002c0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | ATGGC others(973): Show |
chr2 | 183119443 | 183166680 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1545 | 338 | 71 | 54 | 165 | 18 | 28 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0001t0002 | 0/0 | 1545 | 41 | 0 | 4 | 26 | 0 | 11 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0001t0003 | 0/0 | 1545 | 11 | 11 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0001t0004 | 0/0 | 1545 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0001t0005 | 0/0 | 1545 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0001t0006 | 0/0 | 1545 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0002t0001 | 0/0 | 1545 | 4 | 4 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0003t0002 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0001c0004t0001 | 0/0 | 1545 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| a0002c0005t0001 | 0/0 | 1545 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | GTAGT others(1540): Show |
chr2 | 183119443 | 183166680 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| a0002c0005t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0024 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0221 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0292 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0118 | AFR | LWK | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | GIH | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | GIH | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0300 | REF | REF | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | NUP35_chr2_183119443_183166680 | NUP35 | chr2 | 183119443 | 183166680 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:183161061 | C | T | 1 | a0002 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.911C>T | p.Ser304Phe | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 926/1545 | 911/981 | 304/326 | chr2 | 183161061 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:183128357 | A | G | 1 | a0001c0002 | 4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.111A>G | p.Gly37Gly | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/9 | 126/1545 | 111/981 | 37/326 | chr2 | 183128357 | |||
| chr2:183128384 | G | A | 1 | a0001c0003 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.138G>A | p.Pro46Pro | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/9 | 153/1545 | 138/981 | 46/326 | chr2 | 183128384 | |||
| chr2:183159613 | T | C | 1 | a0001c0004 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.864T>C | p.Pro288Pro | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/9 | 879/1545 | 864/981 | 288/326 | chr2 | 183159613 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:183161144 | A | G | 1 | a0001c0001t0006 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 13 | chr2 | 183161144 | ||||||
| chr2:183161147 | G | T | 2 | a0001c0001t0002 a0001c0003t0002 |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*16G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 16 | chr2 | 183161147 | ||||||
| chr2:183161148 | A | T | 2 | a0001c0001t0002 a0001c0003t0002 |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*17A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 17 | chr2 | 183161148 | ||||||
| chr2:183161238 | A | C | 1 | a0001c0001t0005 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 107 | chr2 | 183161238 | ||||||
| chr2:183161260 | T | C | 1 | a0001c0001t0003 | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*129T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 129 | chr2 | 183161260 | ||||||
| chr2:183161340 | C | T | 1 | a0001c0001t0003 | 11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*209C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 209 | chr2 | 183161340 | ||||||
| chr2:183161516 | A | G | 1 | a0001c0001t0004 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*385A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 9/9 | 385 | chr2 | 183161516 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:183124577 | C | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(23): Show |
34 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.40+80C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124577 | |||||||
| chr2:183124651 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.40+154C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124651 | |||||||
| chr2:183124898 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.40+401G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124898 | |||||||
| chr2:183124909 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.40+412C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124909 | |||||||
| chr2:183124916 | GTGTGTGG others(550): Show |
G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.40+422_40+978del | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183124916 | ||||||
| chr2:183124950 | G | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(284): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.40+453G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124950 | |||||||
| chr2:183124988 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.40+491C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183124988 | |||||||
| chr2:183125135 | C | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.40+638C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125135 | |||||||
| chr2:183125242 | G | GA | 13 | a0001c0001t0001g0026 a0001c0001t0001g0071 a0001c0001t0001g0072 others(10): Show |
16 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.40+752dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183125242 | ||||||
| chr2:183125279 | T | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0050 others(5): Show |
13 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+782T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125279 | |||||||
| chr2:183125293 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.40+796G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125293 | |||||||
| chr2:183125351 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+854G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125351 | |||||||
| chr2:183125429 | G | A | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(285): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.40+932G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125429 | |||||||
| chr2:183125497 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.40+1000A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125497 | |||||||
| chr2:183125509 | C | G | 2 | a0001c0001t0001g0119 a0001c0003t0002g0118 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.40+1012C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125509 | |||||||
| chr2:183125560 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(288): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.40+1063T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125560 | |||||||
| chr2:183125698 | TG | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(25): Show |
37 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.40+1205delG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183125698 | ||||||
| chr2:183125762 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.40+1265A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125762 | |||||||
| chr2:183125797 | C | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0295 others(2): Show |
5 | NA18962.hp1 NA19011.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+1300C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125797 | |||||||
| chr2:183125831 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.40+1334G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125831 | |||||||
| chr2:183125837 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0002c0005t0001g0292 |
3 | HG02145.hp1 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.40+1340A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125837 | |||||||
| chr2:183125978 | C | T | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.40+1481C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183125978 | |||||||
| chr2:183126048 | C | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.40+1551C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126048 | |||||||
| chr2:183126071 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.40+1574G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126071 | |||||||
| chr2:183126101 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.40+1604G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126101 | |||||||
| chr2:183126123 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.40+1626C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126123 | |||||||
| chr2:183126124 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.40+1627C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126124 | |||||||
| chr2:183126127 | C | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(37): Show |
68 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.40+1630C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126127 | |||||||
| chr2:183126167 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.40+1670T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126167 | |||||||
| chr2:183126312 | C | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.40+1815C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126312 | |||||||
| chr2:183126320 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.40+1823A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126320 | |||||||
| chr2:183126491 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
53 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.41-1796T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126491 | |||||||
| chr2:183126538 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.41-1749C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126538 | |||||||
| chr2:183126642 | G | GT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0182 a0001c0001t0001g0240 others(4): Show |
11 | HG02165.hp1 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.41-1634dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | ||||||
| chr2:183126642 | G | GTT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(5): Show |
9 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.41-1635_41-1634dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | ||||||
| chr2:183126642 | G | GTTTT | 28 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0002g0003 others(25): Show |
40 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.41-1637_41-1634dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | ||||||
| chr2:183126642 | GT | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.41-1634delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126642 | ||||||
| chr2:183126681 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.41-1606T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126681 | |||||||
| chr2:183126703 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41-1584A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126703 | |||||||
| chr2:183126812 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41-1475A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126812 | |||||||
| chr2:183126836 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1451A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126836 | |||||||
| chr2:183126862 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-1425A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126862 | |||||||
| chr2:183126973 | C | CCTAA | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-1312_41-1311ins others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183126973 | ||||||
| chr2:183126984 | G | GTGCTCAA others(21): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1303_41-1302ins others(28): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126984 | |||||||
| chr2:183126985 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1302G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126985 | |||||||
| chr2:183126986 | T | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1301T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126986 | |||||||
| chr2:183126988 | C | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG01109.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.41-1299C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183126988 | |||||||
| chr2:183127101 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41-1186C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127101 | |||||||
| chr2:183127221 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(97): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.41-1066G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127221 | |||||||
| chr2:183127221 | G | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.41-1066G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127221 | |||||||
| chr2:183127235 | A | G | 1 | a0002c0005t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-1052A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127235 | |||||||
| chr2:183127251 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.41-1036A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127251 | |||||||
| chr2:183127278 | A | AT | 77 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.41-994dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183127278 | ||||||
| chr2:183127373 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.41-914C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127373 | |||||||
| chr2:183127398 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-889G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127398 | |||||||
| chr2:183127401 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.41-886A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127401 | |||||||
| chr2:183127458 | T | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41-829T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127458 | |||||||
| chr2:183127549 | G | T | 1 | a0002c0005t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.41-738G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127549 | |||||||
| chr2:183127555 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.41-732G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127555 | |||||||
| chr2:183127664 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.41-623G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127664 | |||||||
| chr2:183127666 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-621C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127666 | |||||||
| chr2:183127679 | T | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-608T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127679 | |||||||
| chr2:183127779 | A | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-508A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127779 | |||||||
| chr2:183127798 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41-489G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127798 | |||||||
| chr2:183127835 | G | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-452G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127835 | |||||||
| chr2:183127879 | T | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-408T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127879 | |||||||
| chr2:183127880 | C | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41-407C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127880 | |||||||
| chr2:183127884 | G | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-403G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127884 | |||||||
| chr2:183127908 | G | A | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-379G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127908 | |||||||
| chr2:183127929 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(33): Show |
64 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.41-358C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127929 | |||||||
| chr2:183127934 | C | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-353C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127934 | |||||||
| chr2:183127956 | C | G | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41-331C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | chr2 | 183127956 | |||||||
| chr2:183128073 | G | GA | 38 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(35): Show |
51 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.41-201dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183128073 | ||||||
| chr2:183128073 | GA | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(34): Show |
65 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.41-201delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 183128073 | ||||||
| chr2:183128505 | A | G | 31 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(28): Show |
43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.211+48A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128505 | |||||||
| chr2:183128561 | C | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.211+104C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128561 | |||||||
| chr2:183128599 | TA | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(91): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.211+157delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128599 | ||||||
| chr2:183128599 | TAA | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(28): Show |
38 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.211+156_211+157del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128599 | ||||||
| chr2:183128628 | T | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(42): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.211+171T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128628 | |||||||
| chr2:183128713 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+256T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128713 | |||||||
| chr2:183128738 | T | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(216): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.211+281T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128738 | |||||||
| chr2:183128774 | A | ACATT | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+318_211+321dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183128774 | ||||||
| chr2:183128867 | T | A | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+410T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128867 | |||||||
| chr2:183128868 | C | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+411C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128868 | |||||||
| chr2:183128937 | A | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.211+480A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183128937 | |||||||
| chr2:183129039 | C | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+582C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129039 | |||||||
| chr2:183129054 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+597A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129054 | |||||||
| chr2:183129090 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+633A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129090 | |||||||
| chr2:183129201 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211+744C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129201 | |||||||
| chr2:183129217 | T | TG | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.211+767dupG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183129217 | ||||||
| chr2:183129217 | TG | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+767delG | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183129217 | ||||||
| chr2:183129282 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.211+825G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129282 | |||||||
| chr2:183129314 | C | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.211+857C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129314 | |||||||
| chr2:183129412 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.211+955A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129412 | |||||||
| chr2:183129467 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.212-951T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129467 | |||||||
| chr2:183129623 | A | G | 31 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(28): Show |
43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-795A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129623 | |||||||
| chr2:183129726 | C | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.212-692C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129726 | |||||||
| chr2:183129732 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.212-686A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129732 | |||||||
| chr2:183129783 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.212-635G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129783 | |||||||
| chr2:183129880 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.212-538A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183129880 | |||||||
| chr2:183130024 | G | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0047 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.212-394G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130024 | |||||||
| chr2:183130164 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.212-254A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130164 | |||||||
| chr2:183130197 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.212-221T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130197 | |||||||
| chr2:183130217 | C | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-201C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130217 | |||||||
| chr2:183130317 | T | C | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-101T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130317 | |||||||
| chr2:183130347 | A | G | 31 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(28): Show |
43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.212-71A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130347 | |||||||
| chr2:183130355 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-63A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130355 | |||||||
| chr2:183130357 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212-61T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130357 | |||||||
| chr2:183130359 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-59T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130359 | |||||||
| chr2:183130387 | C | CT | 51 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(48): Show |
59 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-12dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | ||||||
| chr2:183130387 | CT | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.212-12delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | ||||||
| chr2:183130387 | CTT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(69): Show |
113 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.212-13_212-12delTT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 183130387 | ||||||
| chr2:183130392 | T | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212-26T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130392 | |||||||
| chr2:183130393 | T | A | 30 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.212-25T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130393 | |||||||
| chr2:183130414 | G | T | 31 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(28): Show |
43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.212-4G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 2/8 | chr2 | 183130414 | |||||||
| chr2:183130614 | C | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.339+69C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130614 | |||||||
| chr2:183130784 | G | T | 31 | a0001c0001t0001g0119 a0001c0001t0002g0003 a0001c0001t0002g0016 others(28): Show |
43 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.339+239G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130784 | |||||||
| chr2:183130808 | C | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.339+263C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130808 | |||||||
| chr2:183130870 | GTTTAATA | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0128 |
3 | NA18969.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.339+338_339+344del others(7): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183130870 | ||||||
| chr2:183130927 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.339+382A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183130927 | |||||||
| chr2:183131001 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+456C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131001 | |||||||
| chr2:183131014 | A | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.339+469A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131014 | |||||||
| chr2:183131146 | A | AT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+610dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183131146 | ||||||
| chr2:183131175 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.339+630G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131175 | |||||||
| chr2:183131193 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.339+648C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131193 | |||||||
| chr2:183131213 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+668C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131213 | |||||||
| chr2:183131247 | ACTTTT | A | 7 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.339+708_339+712del others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183131247 | ||||||
| chr2:183131353 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.339+808G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131353 | |||||||
| chr2:183131767 | A | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.339+1222A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131767 | |||||||
| chr2:183131847 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+1302A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131847 | |||||||
| chr2:183131925 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0006g0024 |
3 | HG01256.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.339+1380T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183131925 | |||||||
| chr2:183132088 | G | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(34): Show |
50 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.340-1478G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132088 | |||||||
| chr2:183132108 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1458C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132108 | |||||||
| chr2:183132332 | T | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1234T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132332 | |||||||
| chr2:183132399 | C | CA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(41): Show |
73 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.340-1156dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183132399 | ||||||
| chr2:183132410 | A | AT | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-1156_340-1155i others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132410 | |||||||
| chr2:183132410 | A | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.340-1156A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132410 | |||||||
| chr2:183132418 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
5 | HG00738.hp2 HG01243.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.340-1148T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132418 | |||||||
| chr2:183132504 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.340-1062G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132504 | |||||||
| chr2:183132513 | G | A | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.340-1053G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132513 | |||||||
| chr2:183132519 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-1047C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132519 | |||||||
| chr2:183132556 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.340-1010C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132556 | |||||||
| chr2:183132655 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.340-911A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132655 | |||||||
| chr2:183132684 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340-882T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132684 | |||||||
| chr2:183132715 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-851A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132715 | |||||||
| chr2:183132896 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.340-670T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183132896 | |||||||
| chr2:183133024 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.340-542T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133024 | |||||||
| chr2:183133036 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.340-530A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133036 | |||||||
| chr2:183133057 | A | G | 1 | a0001c0002t0001g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340-509A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133057 | |||||||
| chr2:183133111 | A | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
4 | HG00323.hp2 HG00642.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-455A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133111 | |||||||
| chr2:183133162 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(80): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.340-404A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133162 | |||||||
| chr2:183133207 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.340-359G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133207 | |||||||
| chr2:183133233 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.340-333T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133233 | |||||||
| chr2:183133323 | C | CT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0128 a0001c0001t0001g0171 others(4): Show |
8 | HG00423.hp2 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.340-228dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | ||||||
| chr2:183133323 | C | CTT | 5 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0172 others(2): Show |
6 | HG01358.hp1 HG01361.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-229_340-228dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | ||||||
| chr2:183133323 | CT | C | 22 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0108 others(19): Show |
25 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.340-228delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | ||||||
| chr2:183133323 | CTT | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(68): Show |
105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.340-229_340-228del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 183133323 | ||||||
| chr2:183133350 | A | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.340-216A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133350 | |||||||
| chr2:183133469 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.340-97A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133469 | |||||||
| chr2:183133509 | C | T | 40 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(37): Show |
47 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.340-57C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133509 | |||||||
| chr2:183133523 | A | G | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.340-43A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 3/8 | chr2 | 183133523 | |||||||
| chr2:183133638 | CT | C | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(134): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.397+32delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183133638 | ||||||
| chr2:183133638 | CTT | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0139 others(4): Show |
8 | HG01517.hp1 HG03491.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.397+31_397+32delTT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183133638 | ||||||
| chr2:183133656 | A | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+33A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133656 | |||||||
| chr2:183133690 | A | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.397+67A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133690 | |||||||
| chr2:183133809 | A | C | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+186A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133809 | |||||||
| chr2:183133884 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+261A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133884 | |||||||
| chr2:183133904 | G | A | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+281G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183133904 | |||||||
| chr2:183134089 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+466G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134089 | |||||||
| chr2:183134136 | T | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+513T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134136 | |||||||
| chr2:183134201 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+578A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134201 | |||||||
| chr2:183134386 | T | A | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+763T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134386 | |||||||
| chr2:183134399 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+776G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | |||||||
| chr2:183134399 | G | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.397+776G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | |||||||
| chr2:183134399 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0113 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.397+776G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134399 | |||||||
| chr2:183134497 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0123 |
3 | HG01975.hp1 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.397+874C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134497 | |||||||
| chr2:183134546 | G | A | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+923G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134546 | |||||||
| chr2:183134553 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+930G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134553 | |||||||
| chr2:183134654 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.397+1031C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134654 | |||||||
| chr2:183134655 | G | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1032G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134655 | |||||||
| chr2:183134723 | C | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+1100C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134723 | |||||||
| chr2:183134764 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.397+1141C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134764 | |||||||
| chr2:183134766 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.397+1143C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134766 | |||||||
| chr2:183134773 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.397+1150G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134773 | |||||||
| chr2:183134782 | A | ATT | 28 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(25): Show |
40 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.397+1173_397+1174d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183134782 | ||||||
| chr2:183134826 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.397+1203G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134826 | |||||||
| chr2:183134870 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+1247C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134870 | |||||||
| chr2:183134916 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+1293G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134916 | |||||||
| chr2:183134925 | G | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+1302G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134925 | |||||||
| chr2:183134958 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1335A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134958 | |||||||
| chr2:183134971 | T | C | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+1348T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183134971 | |||||||
| chr2:183135108 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.397+1485A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135108 | |||||||
| chr2:183135146 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+1523G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135146 | |||||||
| chr2:183135229 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.397+1606T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135229 | |||||||
| chr2:183135289 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+1666C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135289 | |||||||
| chr2:183135415 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
173 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.397+1792G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135415 | |||||||
| chr2:183135439 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+1816G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135439 | |||||||
| chr2:183135464 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1841G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135464 | |||||||
| chr2:183135495 | A | C | 1 | a0001c0001t0001g0168 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.397+1872A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135495 | |||||||
| chr2:183135633 | A | C | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(41): Show |
73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.397+2010A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135633 | |||||||
| chr2:183135676 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.397+2053A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135676 | |||||||
| chr2:183135768 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.397+2145G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135768 | |||||||
| chr2:183135802 | T | A | 1 | a0001c0001t0002g0253 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.397+2179T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135802 | |||||||
| chr2:183135885 | T | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+2262T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183135885 | |||||||
| chr2:183136183 | A | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+2560A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136183 | |||||||
| chr2:183136265 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0200 a0001c0001t0001g0230 others(2): Show |
6 | NA18946.hp2 NA18951.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+2642C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136265 | |||||||
| chr2:183136300 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.397+2677A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136300 | |||||||
| chr2:183136353 | T | C | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+2730T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136353 | |||||||
| chr2:183136585 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.397+2962C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136585 | |||||||
| chr2:183136624 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+3001G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136624 | |||||||
| chr2:183136627 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+3004G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136627 | |||||||
| chr2:183136677 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.397+3054T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136677 | |||||||
| chr2:183136704 | A | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3081A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136704 | |||||||
| chr2:183136755 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0165 a0001c0001t0001g0166 |
4 | HG00673.hp1 HG02071.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+3132A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136755 | |||||||
| chr2:183136815 | C | T | 2 | a0001c0001t0002g0245 a0001c0001t0002g0250 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.397+3192C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136815 | |||||||
| chr2:183136816 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(64): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.397+3193G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183136816 | |||||||
| chr2:183137017 | G | A | 1 | a0001c0001t0001g0017 | 3 | HG00438.hp1 NA18944.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.397+3394G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137017 | |||||||
| chr2:183137071 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+3448T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137071 | |||||||
| chr2:183137080 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.397+3457A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137080 | |||||||
| chr2:183137126 | T | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3503T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137126 | |||||||
| chr2:183137217 | G | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.397+3594G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137217 | |||||||
| chr2:183137279 | G | A | 79 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(76): Show |
99 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.397+3656G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137279 | |||||||
| chr2:183137345 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.397+3722G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137345 | |||||||
| chr2:183137347 | G | C | 1 | a0002c0005t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397+3724G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137347 | |||||||
| chr2:183137398 | A | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+3775A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137398 | |||||||
| chr2:183137399 | G | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+3776G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137399 | |||||||
| chr2:183137478 | C | T | 9 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0101 others(6): Show |
9 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+3855C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137478 | |||||||
| chr2:183137525 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+3902G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137525 | |||||||
| chr2:183137601 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG00735.hp2 HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.397+3978T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137601 | |||||||
| chr2:183137708 | G | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4085G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137708 | |||||||
| chr2:183137739 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0249 a0001c0001t0002g0252 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4116G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137739 | |||||||
| chr2:183137789 | GA | G | 39 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(36): Show |
53 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.397+4177delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183137789 | ||||||
| chr2:183137841 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(221): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.397+4218T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137841 | |||||||
| chr2:183137842 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.397+4219G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137842 | |||||||
| chr2:183137843 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.397+4220G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137843 | |||||||
| chr2:183137860 | A | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+4237A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137860 | |||||||
| chr2:183137914 | A | G | 10 | a0001c0001t0001g0041 a0001c0001t0001g0186 a0001c0001t0001g0222 others(7): Show |
11 | HG00323.hp1 HG00597.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.397+4291A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183137914 | |||||||
| chr2:183138031 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.397+4408A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138031 | |||||||
| chr2:183138146 | G | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(94): Show |
130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.397+4523G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138146 | |||||||
| chr2:183138245 | C | CTA | 4 | a0001c0001t0001g0113 a0001c0001t0001g0197 a0001c0001t0001g0230 others(1): Show |
4 | HG02717.hp1 HG04228.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4646_397+4647d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138245 | ||||||
| chr2:183138245 | C | CTATATAT others(7): Show |
1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.397+4634_397+4647d others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138245 | ||||||
| chr2:183138261 | A | AT | 4 | a0001c0001t0001g0039 a0001c0001t0001g0137 a0001c0001t0001g0164 others(1): Show |
5 | HG02922.hp1 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+4639dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | ||||||
| chr2:183138261 | ATATATAT others(3): Show |
A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0051 others(5): Show |
13 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.397+4640_397+4649d others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | ||||||
| chr2:183138261 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.397+4640_397+4650d others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138261 | ||||||
| chr2:183138263 | A | ATT | 6 | a0001c0001t0001g0248 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01123.hp2 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4641_397+4642i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138263 | ||||||
| chr2:183138263 | A | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0137 a0001c0001t0001g0164 others(1): Show |
5 | HG02922.hp1 HG02970.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.397+4640A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138263 | |||||||
| chr2:183138263 | ATATATAT others(3): Show |
A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(24): Show |
48 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.397+4642_397+4651d others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138263 | ||||||
| chr2:183138265 | A | ATT | 7 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0095 others(4): Show |
7 | HG01069.hp2 HG01515.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | ||||||
| chr2:183138265 | A | ATTT | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | ||||||
| chr2:183138265 | A | ATTTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0092 others(3): Show |
7 | HG00423.hp2 HG00673.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.397+4643_397+4644i others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138265 | ||||||
| chr2:183138265 | A | T | 11 | a0001c0001t0001g0039 a0001c0001t0001g0137 a0001c0001t0001g0164 others(8): Show |
12 | HG01123.hp2 HG02630.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.397+4642A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138265 | |||||||
| chr2:183138267 | A | ATTT | 3 | a0001c0001t0001g0132 a0001c0001t0001g0168 a0001c0001t0001g0173 |
3 | HG01256.hp2 HG02630.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.397+4645_397+4646i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138267 | ||||||
| chr2:183138267 | A | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(90): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.397+4644A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138267 | |||||||
| chr2:183138267 | ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.397+4646_397+4658d others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138267 | ||||||
| chr2:183138269 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0100 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(29): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(27): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(23): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(22): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0098 a0001c0001t0001g0102 |
3 | HG02970.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0070 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0073 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(19): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(8): Show |
2 | a0001c0001t0003g0022 a0001c0001t0003g0023 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0043 a0001c0001t0002g0258 a0001c0001t0002g0260 |
4 | HG03669.hp2 HG03704.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(21): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(3): Show |
1 | a0001c0001t0003g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0023 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(8): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0256 a0001c0001t0003g0075 |
4 | HG02080.hp2 HG02135.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(10): Show |
4 | a0001c0001t0002g0003 a0001c0001t0002g0245 a0001c0001t0002g0268 others(1): Show |
4 | HG02738.hp1 HG03834.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(19): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0044 a0001c0001t0002g0263 |
4 | NA18944.hp2 NA18960.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(21): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0074 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(7): Show |
3 | a0001c0001t0002g0003 a0001c0001t0002g0257 a0001c0001t0002g0266 |
3 | HG02523.hp1 HG03710.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(8): Show |
13 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0044 others(10): Show |
17 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0255 a0001c0001t0002g0265 |
2 | HG02074.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0085 |
3 | HG02486.hp2 HG03209.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATTT others(4): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0038 others(14): Show |
21 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.397+4647_397+4648i others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATATTT others(8): Show |
3 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0264 |
3 | HG00621.hp2 HG02056.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.397+4647_397+4648i others(17): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATTTTT others(3): Show |
1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | ATATTTTT others(4): Show |
1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(13): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138269 | ||||||
| chr2:183138269 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.397+4646A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138269 | |||||||
| chr2:183138270 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.397+4647_397+4648i others(25): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138270 | |||||||
| chr2:183138270 | T | TATATATA others(24): Show |
1 | a0001c0001t0001g0110 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397+4647_397+4648i others(33): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138270 | |||||||
| chr2:183138271 | T | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0114 a0001c0001t0001g0193 others(15): Show |
19 | HG00408.hp2 HG00735.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.397+4648T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138271 | |||||||
| chr2:183138272 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4649T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138272 | |||||||
| chr2:183138273 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.397+4650T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138273 | |||||||
| chr2:183138274 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4651T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138274 | |||||||
| chr2:183138276 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4653T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138276 | |||||||
| chr2:183138278 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.397+4655T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138278 | |||||||
| chr2:183138280 | T | A | 5 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 others(2): Show |
6 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.397+4657T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138280 | |||||||
| chr2:183138356 | G | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.397+4733G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138356 | |||||||
| chr2:183138440 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+4817G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138440 | |||||||
| chr2:183138573 | A | C | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+4950A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138573 | |||||||
| chr2:183138611 | A | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.397+4988A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138611 | |||||||
| chr2:183138615 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.397+4992G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138615 | |||||||
| chr2:183138617 | T | G | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+4994T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138617 | |||||||
| chr2:183138790 | C | CATT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(117): Show |
169 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.397+5168_397+5170d others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138790 | ||||||
| chr2:183138790 | C | CGTT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+5167_397+5168i others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138790 | |||||||
| chr2:183138890 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.397+5267G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138890 | |||||||
| chr2:183138953 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.397+5330A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138953 | |||||||
| chr2:183138971 | G | GCT | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+5353_397+5354d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183138971 | ||||||
| chr2:183138984 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0087 |
3 | HG01884.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.397+5361C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138984 | |||||||
| chr2:183138998 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.397+5375T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138998 | |||||||
| chr2:183138999 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+5376A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183138999 | |||||||
| chr2:183139137 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.397+5514T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139137 | |||||||
| chr2:183139209 | TTTC | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0017 others(20): Show |
45 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.397+5589_397+5591d others(5): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139209 | ||||||
| chr2:183139210 | TTC | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(21): Show |
30 | HG01099.hp2 HG01169.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.397+5589_397+5590d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139210 | ||||||
| chr2:183139211 | TC | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(135): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.397+5589delC | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139211 | |||||||
| chr2:183139212 | C | CT | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+5603dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183139212 | ||||||
| chr2:183139212 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(87): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.397+5589C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139212 | |||||||
| chr2:183139818 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+6195A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139818 | |||||||
| chr2:183139821 | T | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+6198T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139821 | |||||||
| chr2:183139834 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.397+6211T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139834 | |||||||
| chr2:183139844 | T | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.397+6221T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183139844 | |||||||
| chr2:183140352 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.397+6729C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140352 | |||||||
| chr2:183140382 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0143 others(2): Show |
10 | HG02165.hp1 NA18947.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.397+6759T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140382 | |||||||
| chr2:183140451 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.397+6828G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140451 | |||||||
| chr2:183140531 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.397+6908C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140531 | |||||||
| chr2:183140532 | A | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+6909A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140532 | |||||||
| chr2:183140592 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0047 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.397+6969C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140592 | |||||||
| chr2:183140593 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(40): Show |
50 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.397+6970G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140593 | |||||||
| chr2:183140598 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.397+6975G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140598 | |||||||
| chr2:183140629 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+7006C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140629 | |||||||
| chr2:183140804 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.397+7181C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140804 | |||||||
| chr2:183140822 | C | CA | 22 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0026 others(19): Show |
28 | HG00642.hp1 HG01081.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.397+7216dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | ||||||
| chr2:183140822 | C | CAA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(39): Show |
69 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.397+7215_397+7216d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | ||||||
| chr2:183140822 | CA | C | 8 | a0001c0001t0001g0049 a0001c0001t0001g0115 a0001c0001t0001g0138 others(5): Show |
9 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.397+7216delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183140822 | ||||||
| chr2:183140878 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(206): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.397+7255G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140878 | |||||||
| chr2:183140906 | G | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0169 |
2 | HG01361.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.397+7283G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140906 | |||||||
| chr2:183140942 | A | G | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.397+7319A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183140942 | |||||||
| chr2:183141049 | G | T | 1 | a0002c0005t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397+7426G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141049 | |||||||
| chr2:183141096 | T | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7473T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141096 | |||||||
| chr2:183141113 | T | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG00408.hp2 NA18964.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+7490T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141113 | |||||||
| chr2:183141119 | G | GT | 6 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0293 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7509dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183141119 | ||||||
| chr2:183141131 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+7508T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141131 | |||||||
| chr2:183141186 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+7563A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141186 | |||||||
| chr2:183141199 | C | G | 6 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 others(3): Show |
8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.397+7576C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141199 | |||||||
| chr2:183141241 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.397+7618C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141241 | |||||||
| chr2:183141241 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0051 others(6): Show |
14 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.397+7618C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141241 | |||||||
| chr2:183141270 | G | A | 21 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(18): Show |
23 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.397+7647G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141270 | |||||||
| chr2:183141299 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
52 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.397+7676C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141299 | |||||||
| chr2:183141833 | A | G | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.397+8210A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141833 | |||||||
| chr2:183141996 | T | A | 1 | a0001c0001t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.397+8373T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183141996 | |||||||
| chr2:183142116 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.397+8493T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142116 | |||||||
| chr2:183142121 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.397+8498C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142121 | |||||||
| chr2:183142284 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+8661A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142284 | |||||||
| chr2:183142405 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.397+8782A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142405 | |||||||
| chr2:183142408 | T | C | 1 | a0001c0001t0002g0256 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.397+8785T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142408 | |||||||
| chr2:183142415 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.397+8792G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142415 | |||||||
| chr2:183142454 | C | CT | 34 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(31): Show |
47 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.397+8842dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183142454 | ||||||
| chr2:183142468 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.397+8845T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142468 | |||||||
| chr2:183142476 | G | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.397+8853G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142476 | |||||||
| chr2:183142543 | A | G | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.397+8920A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142543 | |||||||
| chr2:183142550 | C | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(39): Show |
49 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.397+8927C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142550 | |||||||
| chr2:183142640 | G | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8868G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142640 | |||||||
| chr2:183142641 | G | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8867G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142641 | |||||||
| chr2:183142644 | T | TA | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-8863dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183142644 | ||||||
| chr2:183142646 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-8862C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142646 | |||||||
| chr2:183142660 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-8848A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142660 | |||||||
| chr2:183142670 | G | A | 6 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 others(3): Show |
8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-8838G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142670 | |||||||
| chr2:183142680 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.398-8828A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142680 | |||||||
| chr2:183142699 | T | C | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-8809T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142699 | |||||||
| chr2:183142702 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-8806A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142702 | |||||||
| chr2:183142713 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8795C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142713 | |||||||
| chr2:183142831 | G | C | 1 | a0002c0005t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.398-8677G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142831 | |||||||
| chr2:183142885 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.398-8623G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142885 | |||||||
| chr2:183142895 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.398-8613G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142895 | |||||||
| chr2:183142934 | G | A | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-8574G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142934 | |||||||
| chr2:183142959 | G | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8549G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183142959 | |||||||
| chr2:183143015 | G | A | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-8493G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143015 | |||||||
| chr2:183143117 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.398-8391C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143117 | |||||||
| chr2:183143141 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8367G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143141 | |||||||
| chr2:183143142 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-8366C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143142 | |||||||
| chr2:183143151 | A | G | 1 | a0001c0002t0001g0046 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.398-8357A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143151 | |||||||
| chr2:183143155 | C | CA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(63): Show |
85 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.398-8338dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183143155 | ||||||
| chr2:183143155 | C | CAA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(45): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-8339_398-8338d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183143155 | ||||||
| chr2:183143166 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-8342A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143166 | |||||||
| chr2:183143175 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
4 | NA18969.hp1 NA18972.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8333A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143175 | |||||||
| chr2:183143176 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
4 | NA18969.hp1 NA18972.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8332G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143176 | |||||||
| chr2:183143178 | A | T | 18 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0101 others(15): Show |
20 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.398-8330A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143178 | |||||||
| chr2:183143263 | G | A | 16 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0101 others(13): Show |
18 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.398-8245G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143263 | |||||||
| chr2:183143293 | T | TC | 80 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(77): Show |
101 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.398-8215_398-8214i others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143293 | |||||||
| chr2:183143293 | T | TTC | 46 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-8215_398-8214i others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143293 | |||||||
| chr2:183143295 | C | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-8213C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143295 | |||||||
| chr2:183143295 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.398-8213C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143295 | |||||||
| chr2:183143481 | G | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-8027G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143481 | |||||||
| chr2:183143703 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-7805C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143703 | |||||||
| chr2:183143724 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-7784A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143724 | |||||||
| chr2:183143878 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0227 |
2 | HG00597.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.398-7630A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183143878 | |||||||
| chr2:183144002 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(42): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-7506A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144002 | |||||||
| chr2:183144080 | G | T | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-7428G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144080 | |||||||
| chr2:183144236 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-7272A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144236 | |||||||
| chr2:183144334 | A | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-7174A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144334 | |||||||
| chr2:183144342 | G | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.398-7166G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144342 | |||||||
| chr2:183144400 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.398-7108C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144400 | |||||||
| chr2:183144476 | G | A | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-7032G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144476 | |||||||
| chr2:183144588 | T | TAATAAG | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-6919_398-6914d others(8): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183144588 | ||||||
| chr2:183144673 | C | T | 1 | a0001c0004t0001g0221 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.398-6835C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144673 | |||||||
| chr2:183144682 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.398-6826G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144682 | |||||||
| chr2:183144748 | T | C | 2 | a0001c0001t0003g0093 a0001c0001t0003g0094 |
2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.398-6760T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144748 | |||||||
| chr2:183144804 | T | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(35): Show |
66 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.398-6704T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144804 | |||||||
| chr2:183144948 | A | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.398-6560A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144948 | |||||||
| chr2:183144995 | A | C | 3 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 |
3 | NA18951.hp1 NA18966.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.398-6513A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183144995 | |||||||
| chr2:183145243 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(121): Show |
174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.398-6265C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145243 | |||||||
| chr2:183145263 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0301 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.398-6245A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145263 | |||||||
| chr2:183145277 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0201 a0001c0001t0001g0208 others(2): Show |
6 | HG00438.hp2 HG02040.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.398-6231G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145277 | |||||||
| chr2:183145307 | G | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(34): Show |
65 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.398-6201G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145307 | |||||||
| chr2:183145350 | T | C | 12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0098 others(9): Show |
12 | HG01255.hp1 HG01261.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.398-6158T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145350 | |||||||
| chr2:183145361 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-6147T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145361 | |||||||
| chr2:183145544 | CACATGTA others(6): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-5959_398-5947d others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183145544 | ||||||
| chr2:183145764 | A | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-5744A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145764 | |||||||
| chr2:183145873 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.398-5635G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145873 | |||||||
| chr2:183145931 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.398-5577A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145931 | |||||||
| chr2:183145967 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.398-5541A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183145967 | |||||||
| chr2:183146030 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-5478G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146030 | |||||||
| chr2:183146033 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.398-5475C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146033 | |||||||
| chr2:183146142 | A | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-5366A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146142 | |||||||
| chr2:183146150 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5358C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146150 | |||||||
| chr2:183146235 | C | CA | 8 | a0001c0001t0001g0049 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
9 | HG00642.hp2 HG01099.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.398-5263dupA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183146235 | ||||||
| chr2:183146252 | C | A | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-5256C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146252 | |||||||
| chr2:183146257 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-5251A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146257 | |||||||
| chr2:183146276 | G | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0260 |
3 | HG03669.hp2 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.398-5232G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146276 | |||||||
| chr2:183146329 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0160 a0001c0001t0001g0162 others(1): Show |
4 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-5179C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146329 | |||||||
| chr2:183146653 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.398-4855G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146653 | |||||||
| chr2:183146660 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(42): Show |
75 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.398-4848G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146660 | |||||||
| chr2:183146679 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(90): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.398-4829C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146679 | |||||||
| chr2:183146782 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.398-4726A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146782 | |||||||
| chr2:183146794 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.398-4714G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146794 | |||||||
| chr2:183146887 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA19062.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.398-4621C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183146887 | |||||||
| chr2:183147169 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.398-4339G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147169 | |||||||
| chr2:183147202 | T | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-4306T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147202 | |||||||
| chr2:183147251 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
27 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.398-4257C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147251 | |||||||
| chr2:183147261 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(123): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.398-4247T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147261 | |||||||
| chr2:183147320 | T | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(33): Show |
63 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.398-4188T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147320 | |||||||
| chr2:183147383 | G | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-4125G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147383 | |||||||
| chr2:183147408 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0123 |
3 | HG01975.hp1 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.398-4100G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147408 | |||||||
| chr2:183147423 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0301 |
2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.398-4085A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147423 | |||||||
| chr2:183147583 | T | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
29 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.398-3925T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147583 | |||||||
| chr2:183147592 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.398-3916A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147592 | |||||||
| chr2:183147667 | T | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-3841T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147667 | |||||||
| chr2:183147766 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.398-3742T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147766 | |||||||
| chr2:183147866 | T | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-3642T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183147866 | |||||||
| chr2:183147915 | A | AT | 32 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0002g0003 others(29): Show |
45 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.398-3580dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183147915 | ||||||
| chr2:183147915 | AT | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
76 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.398-3580delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183147915 | ||||||
| chr2:183148006 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-3502A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148006 | |||||||
| chr2:183148007 | C | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-3501C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148007 | |||||||
| chr2:183148037 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.398-3471C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148037 | |||||||
| chr2:183148204 | C | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-3304C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148204 | |||||||
| chr2:183148306 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0286 |
4 | NA18961.hp2 NA18999.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.398-3202G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148306 | |||||||
| chr2:183148402 | G | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(11): Show |
20 | HG00408.hp1 HG02015.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.398-3106G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148402 | |||||||
| chr2:183148563 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(41): Show |
73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.398-2945T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148563 | |||||||
| chr2:183148610 | ATTCATGT others(11): Show |
A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0079 others(8): Show |
14 | HG00099.hp2 HG00741.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.398-2894_398-2877d others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183148610 | ||||||
| chr2:183148634 | T | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-2874T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148634 | |||||||
| chr2:183148799 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.398-2709C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148799 | |||||||
| chr2:183148807 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.398-2701C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148807 | |||||||
| chr2:183148815 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.398-2693C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148815 | |||||||
| chr2:183148821 | G | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2687G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148821 | |||||||
| chr2:183148890 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.398-2618C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148890 | |||||||
| chr2:183148905 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.398-2603C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148905 | |||||||
| chr2:183148906 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00735.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.398-2602G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148906 | |||||||
| chr2:183148910 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-2598G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148910 | |||||||
| chr2:183148922 | C | T | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.398-2586C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148922 | |||||||
| chr2:183148958 | A | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-2550A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148958 | |||||||
| chr2:183148968 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.398-2540C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148968 | |||||||
| chr2:183148978 | A | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.398-2530A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183148978 | |||||||
| chr2:183149193 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.398-2315G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149193 | |||||||
| chr2:183149203 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.398-2305G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149203 | |||||||
| chr2:183149281 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.398-2227A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149281 | |||||||
| chr2:183149306 | CAAAATTT | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0079 a0001c0001t0006g0024 |
3 | HG01256.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.398-2192_398-2186d others(9): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183149306 | ||||||
| chr2:183149314 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-2194A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149314 | |||||||
| chr2:183149353 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.398-2155C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149353 | |||||||
| chr2:183149436 | G | GT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.398-2068dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183149436 | ||||||
| chr2:183149469 | A | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.398-2039A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149469 | |||||||
| chr2:183149510 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0113 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.398-1998C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149510 | |||||||
| chr2:183149529 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.398-1979T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149529 | |||||||
| chr2:183149867 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01358.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.398-1641C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149867 | |||||||
| chr2:183149909 | T | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(94): Show |
117 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.398-1599T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183149909 | |||||||
| chr2:183150135 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.398-1373G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150135 | |||||||
| chr2:183150210 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(45): Show |
78 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.398-1298A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150210 | |||||||
| chr2:183150237 | G | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG00735.hp2 HG01257.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1271G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150237 | |||||||
| chr2:183150285 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-1223C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150285 | |||||||
| chr2:183150361 | G | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(276): Show |
373 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.398-1147G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150361 | |||||||
| chr2:183150375 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.398-1133T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150375 | |||||||
| chr2:183150383 | C | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.398-1125C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150383 | |||||||
| chr2:183150422 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.398-1086A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150422 | |||||||
| chr2:183150486 | C | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.398-1022C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150486 | |||||||
| chr2:183150544 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.398-964A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150544 | |||||||
| chr2:183150560 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.398-948A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150560 | |||||||
| chr2:183150618 | CTG | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-888_398-887del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 183150618 | ||||||
| chr2:183150873 | A | G | 9 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 others(6): Show |
11 | HG02257.hp2 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.398-635A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150873 | |||||||
| chr2:183150890 | A | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.398-618A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183150890 | |||||||
| chr2:183151053 | G | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-455G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151053 | |||||||
| chr2:183151065 | T | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01175.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.398-443T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151065 | |||||||
| chr2:183151115 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.398-393C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151115 | |||||||
| chr2:183151291 | A | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.398-217A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151291 | |||||||
| chr2:183151385 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-123G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151385 | |||||||
| chr2:183151417 | T | C | 6 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 others(3): Show |
8 | HG02257.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.398-91T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151417 | |||||||
| chr2:183151462 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.398-46C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151462 | |||||||
| chr2:183151500 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG01515.hp2 | splice_region_variant&intron_variant | LOW | c.398-8T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 4/8 | chr2 | 183151500 | |||||||
| chr2:183151664 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+15C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151664 | |||||||
| chr2:183151873 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+224C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151873 | |||||||
| chr2:183151899 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
76 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.539+250A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151899 | |||||||
| chr2:183151939 | A | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(258): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.539+290A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183151939 | |||||||
| chr2:183152063 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0033 others(24): Show |
35 | HG00408.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.539+414A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152063 | |||||||
| chr2:183152068 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539+419G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152068 | |||||||
| chr2:183152110 | A | AAC | 24 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0039 others(21): Show |
32 | HG00140.hp2 HG00323.hp1 HG02074.hp1 others(29): Show |
intron_variant | MODIFIER | c.539+505_539+506dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACAC | 27 | a0001c0001t0001g0072 a0001c0001t0001g0095 a0001c0001t0001g0103 others(24): Show |
30 | HG01069.hp2 HG01255.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.539+503_539+506dup others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACAC | 24 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0069 others(21): Show |
28 | HG00741.hp1 HG01071.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.539+501_539+506dup others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(1): Show |
20 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0147 others(17): Show |
24 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.539+499_539+506dup others(8): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(3): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0070 others(14): Show |
23 | HG00408.hp2 HG02015.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.539+497_539+506dup others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(5): Show |
6 | a0001c0001t0001g0193 a0001c0001t0001g0200 a0001c0001t0001g0212 others(3): Show |
6 | HG01928.hp1 HG02698.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+495_539+506dup others(12): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(7): Show |
8 | a0001c0001t0001g0040 a0001c0001t0001g0068 a0001c0001t0001g0183 others(5): Show |
9 | HG00140.hp1 HG00609.hp2 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.539+493_539+506dup others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(9): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0211 a0001c0001t0001g0236 others(1): Show |
5 | HG00558.hp1 HG02300.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+491_539+506dup others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | AACACACA others(11): Show |
2 | a0001c0001t0001g0222 a0001c0001t0001g0235 |
2 | HG02132.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.539+489_539+506dup others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0219 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.539+461_539+462ins others(11): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152110 | |||||||
| chr2:183152110 | A | ACACACAC others(8): Show |
1 | a0001c0001t0001g0226 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.539+461_539+462ins others(15): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152110 | |||||||
| chr2:183152110 | AAC | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0025 others(36): Show |
54 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.539+505_539+506del others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACAC | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0034 others(23): Show |
30 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.539+503_539+506del others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACAC | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0101 a0001c0001t0001g0184 |
3 | HG01255.hp1 HG02622.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.539+501_539+506del others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACACA others(3): Show |
A | 1 | a0001c0001t0003g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.539+497_539+506del others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACACA others(7): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.539+493_539+506del others(14): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACACA others(9): Show |
A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+491_539+506del others(16): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACACA others(11): Show |
A | 4 | a0001c0001t0001g0168 a0001c0002t0001g0020 a0001c0002t0001g0046 others(1): Show |
5 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+489_539+506del others(18): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152110 | AACACACA others(13): Show |
A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.539+487_539+506del others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152110 | ||||||
| chr2:183152143 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.539+494A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152143 | |||||||
| chr2:183152156 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.539+507A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152156 | |||||||
| chr2:183152189 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(274): Show |
371 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.539+540G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152189 | |||||||
| chr2:183152193 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.539+544T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152193 | |||||||
| chr2:183152209 | C | CAG | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.539+561_539+562dup others(2): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183152209 | ||||||
| chr2:183152272 | C | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(47): Show |
80 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.539+623C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152272 | |||||||
| chr2:183152281 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.539+632A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152281 | |||||||
| chr2:183152347 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.539+698T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152347 | |||||||
| chr2:183152382 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(91): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.539+733T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152382 | |||||||
| chr2:183152396 | G | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(276): Show |
373 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.539+747G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152396 | |||||||
| chr2:183152451 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+802C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152451 | |||||||
| chr2:183152769 | A | T | 2 | a0001c0001t0004g0028 a0001c0001t0004g0116 |
3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.539+1120A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152769 | |||||||
| chr2:183152796 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539+1147T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152796 | |||||||
| chr2:183152849 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.539+1200A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152849 | |||||||
| chr2:183152862 | AT | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1214delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152862 | |||||||
| chr2:183152878 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0138 a0001c0001t0001g0158 |
5 | NA18965.hp1 NA18993.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1229A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183152878 | |||||||
| chr2:183153027 | A | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.539+1378A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153027 | |||||||
| chr2:183153068 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.539+1419A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153068 | |||||||
| chr2:183153164 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.539+1515G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153164 | |||||||
| chr2:183153192 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.539+1543C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153192 | |||||||
| chr2:183153250 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(255): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.539+1601A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153250 | |||||||
| chr2:183153281 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(44): Show |
77 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.539+1632C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153281 | |||||||
| chr2:183153448 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.539+1799A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153448 | |||||||
| chr2:183153466 | C | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+1817C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153466 | |||||||
| chr2:183153602 | C | T | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.539+1953C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153602 | |||||||
| chr2:183153623 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.539+1974C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153623 | |||||||
| chr2:183153677 | C | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+2028C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153677 | |||||||
| chr2:183153801 | A | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0222 a0001c0001t0001g0228 others(1): Show |
5 | HG02132.hp2 NA18982.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+2152A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153801 | |||||||
| chr2:183153890 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(44): Show |
77 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.539+2241C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153890 | |||||||
| chr2:183153931 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.539+2282A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183153931 | |||||||
| chr2:183154019 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.539+2370A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154019 | |||||||
| chr2:183154067 | T | TC | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.539+2422dupC | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183154067 | ||||||
| chr2:183154084 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.539+2435C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154084 | |||||||
| chr2:183154098 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.539+2449A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154098 | |||||||
| chr2:183154116 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
4 | HG01261.hp1 HG02258.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+2467C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154116 | |||||||
| chr2:183154152 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.539+2503C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154152 | |||||||
| chr2:183154199 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.539+2550T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154199 | |||||||
| chr2:183154239 | T | C | 2 | a0001c0002t0001g0046 a0001c0002t0001g0047 |
2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.539+2590T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154239 | |||||||
| chr2:183154342 | C | T | 1 | a0001c0002t0001g0020 | 2 | HG02257.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.539+2693C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154342 | |||||||
| chr2:183154426 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.539+2777T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154426 | |||||||
| chr2:183154434 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.539+2785C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154434 | |||||||
| chr2:183154550 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.540-2894C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154550 | |||||||
| chr2:183154577 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG02895.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.540-2867A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154577 | |||||||
| chr2:183154618 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.540-2826C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154618 | |||||||
| chr2:183154715 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540-2729C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154715 | |||||||
| chr2:183154737 | G | C | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.540-2707G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154737 | |||||||
| chr2:183154948 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.540-2496C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154948 | |||||||
| chr2:183154993 | G | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.540-2451G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183154993 | |||||||
| chr2:183155010 | A | C | 1 | a0001c0004t0001g0221 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.540-2434A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155010 | |||||||
| chr2:183155013 | TACTC | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-2427_540-2424d others(6): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155013 | ||||||
| chr2:183155218 | C | G | 29 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(26): Show |
41 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.540-2226C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155218 | |||||||
| chr2:183155322 | A | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-2122A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155322 | |||||||
| chr2:183155344 | T | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0301 others(2): Show |
6 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-2100T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155344 | |||||||
| chr2:183155579 | C | CT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.540-1851dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | ||||||
| chr2:183155579 | C | CTT | 13 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0117 others(10): Show |
14 | HG00408.hp2 HG01099.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.540-1852_540-1851d others(4): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | ||||||
| chr2:183155579 | CT | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0101 others(4): Show |
7 | HG00621.hp2 HG01255.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.540-1851delT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183155579 | ||||||
| chr2:183155682 | C | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1762C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155682 | |||||||
| chr2:183155703 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.540-1741T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155703 | |||||||
| chr2:183155758 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-1686C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155758 | |||||||
| chr2:183155776 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0087 |
2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.540-1668A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155776 | |||||||
| chr2:183155862 | G | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0243 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.540-1582G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155862 | |||||||
| chr2:183155874 | C | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(41): Show |
73 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.540-1570C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155874 | |||||||
| chr2:183155907 | A | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.540-1537A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155907 | |||||||
| chr2:183155913 | C | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-1531C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183155913 | |||||||
| chr2:183156093 | A | G | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-1351A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156093 | |||||||
| chr2:183156162 | A | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-1282A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156162 | |||||||
| chr2:183156219 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.540-1225C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156219 | |||||||
| chr2:183156347 | T | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-1097T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156347 | |||||||
| chr2:183156406 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-1038C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156406 | |||||||
| chr2:183156443 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.540-1001G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156443 | |||||||
| chr2:183156484 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(77): Show |
122 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.540-960T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156484 | |||||||
| chr2:183156520 | T | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0115 a0001c0001t0001g0301 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.540-924T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156520 | |||||||
| chr2:183156607 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.540-837C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156607 | |||||||
| chr2:183156634 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0073 |
5 | HG02257.hp2 HG02559.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.540-810C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156634 | |||||||
| chr2:183156695 | A | AT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(81): Show |
127 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.540-738dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 183156695 | ||||||
| chr2:183156753 | A | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.540-691A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156753 | |||||||
| chr2:183156763 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(275): Show |
372 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.540-681G>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156763 | |||||||
| chr2:183156773 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-671G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156773 | |||||||
| chr2:183156810 | A | G | 6 | a0001c0001t0001g0248 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01123.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.540-634A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156810 | |||||||
| chr2:183156813 | C | G | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-631C>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156813 | |||||||
| chr2:183156940 | T | G | 1 | a0001c0003t0002g0118 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.540-504T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183156940 | |||||||
| chr2:183157052 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(43): Show |
75 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.540-392A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157052 | |||||||
| chr2:183157179 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-265C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157179 | |||||||
| chr2:183157287 | G | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.540-157G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157287 | |||||||
| chr2:183157384 | A | G | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-60A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 5/8 | chr2 | 183157384 | |||||||
| chr2:183157590 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.609+77A>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157590 | |||||||
| chr2:183157665 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+152G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157665 | |||||||
| chr2:183157717 | T | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.609+204T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157717 | |||||||
| chr2:183157726 | T | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0297 |
2 | NA18962.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.609+213T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157726 | |||||||
| chr2:183157760 | C | T | 36 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(33): Show |
49 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.609+247C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183157760 | |||||||
| chr2:183158011 | T | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0197 a0001c0001t0001g0198 others(12): Show |
16 | HG00408.hp2 HG00438.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.610-272T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183158011 | |||||||
| chr2:183158048 | C | CATT | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.610-233_610-232ins others(3): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 183158048 | ||||||
| chr2:183158207 | CCTATTTT others(15): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.610-75_610-54delCT others(20): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 6/8 | chr2 | 183158207 | |||||||
| chr2:183158423 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.738+12G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158423 | |||||||
| chr2:183158567 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.738+156G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158567 | |||||||
| chr2:183158649 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.738+238C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158649 | |||||||
| chr2:183158870 | T | C | 1 | a0001c0001t0002g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.738+459T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158870 | |||||||
| chr2:183158876 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.738+465T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158876 | |||||||
| chr2:183158922 | G | C | 1 | a0001c0001t0003g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.738+511G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183158922 | |||||||
| chr2:183159014 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.739-474A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159014 | |||||||
| chr2:183159156 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
352 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.739-332C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159156 | |||||||
| chr2:183159227 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.739-261T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159227 | |||||||
| chr2:183159238 | T | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.739-250T>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159238 | |||||||
| chr2:183159298 | T | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
374 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.739-190T>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159298 | |||||||
| chr2:183159415 | T | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(89): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.739-73T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159415 | |||||||
| chr2:183159462 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(47): Show |
80 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.739-26A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 7/8 | chr2 | 183159462 | |||||||
| chr2:183159734 | G | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.903+82G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159734 | |||||||
| chr2:183159783 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0013 others(38): Show |
69 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.903+131T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159783 | |||||||
| chr2:183159858 | A | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.903+206A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159858 | |||||||
| chr2:183159962 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0016 a0001c0001t0002g0043 others(27): Show |
42 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.903+310C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159962 | |||||||
| chr2:183159965 | ATTAAAAC others(3): Show |
A | 1 | a0001c0001t0001g0185 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.903+314_903+323del others(10): Show |
NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159965 | |||||||
| chr2:183159974 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.903+322T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183159974 | |||||||
| chr2:183160011 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.903+359G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160011 | |||||||
| chr2:183160042 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.903+390T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160042 | |||||||
| chr2:183160053 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.903+401A>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160053 | |||||||
| chr2:183160094 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.903+442A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160094 | |||||||
| chr2:183160315 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+663G>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160315 | |||||||
| chr2:183160410 | C | T | 6 | a0001c0001t0001g0049 a0001c0001t0001g0110 a0001c0001t0001g0115 others(3): Show |
7 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.904-644C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160410 | |||||||
| chr2:183160447 | G | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0046 a0001c0002t0001g0047 |
4 | HG02257.hp1 HG02280.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-607G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160447 | |||||||
| chr2:183160550 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(172): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.904-504T>C | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160550 | |||||||
| chr2:183160670 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-384C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160670 | |||||||
| chr2:183160804 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.904-250C>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160804 | |||||||
| chr2:183160805 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.904-249G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160805 | |||||||
| chr2:183160848 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.904-206C>T | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160848 | |||||||
| chr2:183160995 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-59G>A | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160995 | |||||||
| chr2:183160999 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.904-55A>G | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | chr2 | 183160999 | |||||||
| chr2:183161022 | TA | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0120 others(1): Show |
5 | HG00280.hp2 HG00639.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.904-30delA | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 183161022 | ||||||
| chr2:183161027 | G | GT | 7 | a0001c0001t0001g0117 a0001c0001t0001g0145 a0001c0001t0001g0214 others(4): Show |
7 | HG00423.hp1 HG00621.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.904-19dupT | NUP35 | ENSG00000163002.13 | transcript | ENST00000295119.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 183161027 |